SNPedia (pronounced "snipedia") is a wiki-based bioinformatics web site that serves as a database of single nucleotide polymorphisms (SNPs). Each article

PMID 18033686. "rs671 is a classic SNP (Single Nucleotide Polymorphism)". SNPedia. 18 November 2020. Archived from the original on 2018-10-22. "Esophageal

MediaWiki. Other public wikis that run on MediaWiki include wikiHow and SNPedia. WikiLeaks began as a MediaWiki-based site, but is no longer a wiki. A

Leiden, Arg506Gln, R506Q, G1691A Gene Factor V Chromosome 1 External databases Ensembl Human SNPView dbSNP 6025 HapMap 6025 SNPedia 6025 ALFRED SI001216K

3109/00048679809062742. PMID 9588310. S2CID 34824025. "Rs2032583 -SNPedia". Snpedia.com. Archived from the original on 11 December 2013. Retrieved 21

SNPedia ( http://www.SNPedia.com ) is a wiki resource of the functional consequences of human genetic variation as published in peer-reviewed studies. Onl…

SNPedia SNPedia is a wiki investigating human genetics. We share information about the effects of variations in DNA, citing peer-reviewed scientific publ…

SNPedia has been launched to help realize the potential of the Human Genome Project to connect to our daily lives and well-being. Our genes are important…

SNPedia (pronounced "snipedia") is a wiki-based bioinformatics web site that serves as a database of single nucleotide polymorphisms (SNPs). Each article…

SNPedia (pronounced "snipedia") is a wiki-based bioinformatics web site that serves as a database of single nucleotide polymorphisms (SNPs). Each article…

SNPedia (pronounced "snipedia") is a wiki-based bioinformatics web site that serves as a database of single nucleotide polymorphisms (SNPs). Each article…

SNPedia has been launched to help realize the potential of the Human Genome Project to connect to our daily lives and well-being. Our genes are important,…

Status: The MediaWiki API is a mature and stable interface that is actively supported and improved. While we try to avoid it, we may occasionally need to …

rs671 is a classic SNP, well known in a sense through the phenomena known as the "alcohol flush", also known as the "Asian Flush" or "Asian blush", in whi…

Does the CCR5-delta32 mutation have an entirely positive/protective role? Probably not. In patients with abdominal aortic aneurysm (AAA), the major risk i…

Only individuals homozygous for this allele, in other words having the rs334(T;T) genotype, will have sickle cell anemia . The (T) allele appears to have …

GRCh38 is the Genome Reference Consortium Human genome build 38. As of May 7, 2014 it is the standard reference assembly sequence used by NCBI . Unlike ot…

[3] Carrying two copies of a common variant of TCF7L2 doubles your chances of developing Type-2 diabetes and puts you in a similar risk category to being …

rs5498 , also known as E469K or K469E, is a SNP in the ICAM1 gene that has been associated in some studies (and not others) with risk for type-1 diabetes …

At the beginning of SNPedia, public genomic data was rare and this page was useful. Overtime many sources of public genomes have become available, as ment…

rs4680 (Val158Met) is a well studied SNP in the COMT gene. The COMT gene codes for the COMT enzyme, which breaks down dopamine in the brain's prefrontal c…

A genoset refers to a defined set of genotypes ; we have coined the term to represent the combination of alleles at 2 or more loci, especially when they a…

Male pattern baldness , sometimes abbreviated MPB and referred to clinically as androgenetic alopecia, is thought to affect up to 80% of all males by the …

[ PMID 17211608 ] 1,073 men and 1,207 women participating in the Framingham Offspring Study rs662799 -1131T>C in modulates the effect of fat intake on BMI…

This SNP, located in the fourth exon of the ApoE gene, affects the amino acid at position 130 of the resulting protein. The more common rs429358 allele is…

[ PMID 18262040 ] rs599839 and rs4970834 explain about 1% of the variation in circulating LDL-cholesterol levels. "When we look at this particular genetic…

As most commonly used within SNPedia, genotype refers to the pair of SNPs inherited at a given chromosomal position, one inherited from Dad, one inherited…

DNA.land is a service that takes a person's genomic DNA data files from companies such as 23andMe, Ancestry.com, and FamilyTreeDNA for ancestry and possib…

Note: this is one of two SNPs within the TCF7L2 gene that have been reported to be associated with type-2 diabetes, the other being rs4506565. They have …

Magnitude is a subjective measure of interest varying from 0 to 10. Over time it should be adjusted up or down by the community. It is generally interpret…

The rs1799971 (G) allele in exon 1 of the mu opioid receptor OPRM1 gene causes the normal amino acid at residue 40, asparagine (Asn), to be replaced by as…

The most common nucleotide at this position, (C), encodes an arginine (amino acid code R), the alternative T allele encodes a stop codon (X). Hence, the S…

The allele associated with red hair and increased anesthetic response (when homozygous) is rs1805007(T); the wild-type, more common allele is rs1805007(C…

This SNP is 1 of 3 SNPs defining a haplotype that has been studied for association with eye color . The full details on the correspondence between the hap…

A SNP in rs1229984 encodes a form of the alcohol dehydrogenase ADH1B gene that significantly reduces the clearance rate of alcohol from the liver. This SN…

We are fast approaching an era in which genetic information is no longer exclusive or medicalized. Instead, as screening costs plummet and our knowledge …

Contents SNPedia is a Semantic MediaWiki-based wiki investigating human genetics. We keep track of all of the scientific literature known about each posi…

SNPedia (pronounced "snipedia") is a wiki-based bioinformatics web site that serves as a database of single nucleotide polymorphisms (SNPs). Each article…

Links to SNPedia Note: For some SNPs, testing providers detect the genotype from the opposite strand of DNA, so that the genotypes listed on openSNP don'…

Links to SNPedia Note: For some SNPs, testing providers detect the genotype from the opposite strand of DNA, so that the genotypes listed on openSNP don'…

Links to SNPedia Note: For some SNPs, testing providers detect the genotype from the opposite strand of DNA, so that the genotypes listed on openSNP don'…

Links to SNPedia Note: For some SNPs, testing providers detect the genotype from the opposite strand of DNA, so that the genotypes listed on openSNP don'…

Links to SNPedia Note: For some SNPs, testing providers detect the genotype from the opposite strand of DNA, so that the genotypes listed on openSNP don'…

SNPedia (pronounced "snipedia") is a wiki-based bioinformatics web site that serves as a database of single nucleotide polymorphisms (SNPs). Each article

SNPedia SNPedia is a wiki investigating human genetics. We share information about the effects of variations in DNA, citing peer-reviewed scientific publi…

PMID 18033686. "rs671 is a classic SNP (Single Nucleotide Polymorphism)". SNPedia. 18 November 2020. Archived from the original on 2018-10-22. "Esophageal

MediaWiki. Other public wikis that run on MediaWiki include wikiHow and SNPedia. WikiLeaks began as a MediaWiki-based site, but is no longer a wiki. A

Leiden, Arg506Gln, R506Q, G1691A Gene Factor V Chromosome 1 External databases Ensembl Human SNPView dbSNP 6025 HapMap 6025 SNPedia 6025 ALFRED SI001216K

3109/00048679809062742. PMID 9588310. S2CID 34824025. "Rs2032583 -SNPedia". Snpedia.com. Archived from the original on 11 December 2013. Retrieved 21

SNPedia ( http://www.SNPedia.com ) is a wiki resource of the functional consequences of human genetic variation as published in peer-reviewed studies. Onl…

SNPedia SNPedia is a wiki investigating human genetics. We share information about the effects of variations in DNA, citing peer-reviewed scientific publ…

SNPedia has been launched to help realize the potential of the Human Genome Project to connect to our daily lives and well-being. Our genes are important…

SNPedia (pronounced "snipedia") is a wiki-based bioinformatics web site that serves as a database of single nucleotide polymorphisms (SNPs). Each article…

SNPedia (pronounced "snipedia") is a wiki-based bioinformatics web site that serves as a database of single nucleotide polymorphisms (SNPs). Each article…

SNPedia (pronounced "snipedia") is a wiki-based bioinformatics web site that serves as a database of single nucleotide polymorphisms (SNPs). Each article…

SNPedia has been launched to help realize the potential of the Human Genome Project to connect to our daily lives and well-being. Our genes are important,…

Status: The MediaWiki API is a mature and stable interface that is actively supported and improved. While we try to avoid it, we may occasionally need to …

rs671 is a classic SNP, well known in a sense through the phenomena known as the "alcohol flush", also known as the "Asian Flush" or "Asian blush", in whi…

Does the CCR5-delta32 mutation have an entirely positive/protective role? Probably not. In patients with abdominal aortic aneurysm (AAA), the major risk i…

Only individuals homozygous for this allele, in other words having the rs334(T;T) genotype, will have sickle cell anemia . The (T) allele appears to have …

GRCh38 is the Genome Reference Consortium Human genome build 38. As of May 7, 2014 it is the standard reference assembly sequence used by NCBI . Unlike ot…

[3] Carrying two copies of a common variant of TCF7L2 doubles your chances of developing Type-2 diabetes and puts you in a similar risk category to being …

rs5498 , also known as E469K or K469E, is a SNP in the ICAM1 gene that has been associated in some studies (and not others) with risk for type-1 diabetes …

At the beginning of SNPedia, public genomic data was rare and this page was useful. Overtime many sources of public genomes have become available, as ment…

rs4680 (Val158Met) is a well studied SNP in the COMT gene. The COMT gene codes for the COMT enzyme, which breaks down dopamine in the brain's prefrontal c…

A genoset refers to a defined set of genotypes ; we have coined the term to represent the combination of alleles at 2 or more loci, especially when they a…

Male pattern baldness , sometimes abbreviated MPB and referred to clinically as androgenetic alopecia, is thought to affect up to 80% of all males by the …

[ PMID 17211608 ] 1,073 men and 1,207 women participating in the Framingham Offspring Study rs662799 -1131T>C in modulates the effect of fat intake on BMI…

This SNP, located in the fourth exon of the ApoE gene, affects the amino acid at position 130 of the resulting protein. The more common rs429358 allele is…

[ PMID 18262040 ] rs599839 and rs4970834 explain about 1% of the variation in circulating LDL-cholesterol levels. "When we look at this particular genetic…

As most commonly used within SNPedia, genotype refers to the pair of SNPs inherited at a given chromosomal position, one inherited from Dad, one inherited…

DNA.land is a service that takes a person's genomic DNA data files from companies such as 23andMe, Ancestry.com, and FamilyTreeDNA for ancestry and possib…

Note: this is one of two SNPs within the TCF7L2 gene that have been reported to be associated with type-2 diabetes, the other being rs4506565. They have …

Magnitude is a subjective measure of interest varying from 0 to 10. Over time it should be adjusted up or down by the community. It is generally interpret…

The rs1799971 (G) allele in exon 1 of the mu opioid receptor OPRM1 gene causes the normal amino acid at residue 40, asparagine (Asn), to be replaced by as…

The most common nucleotide at this position, (C), encodes an arginine (amino acid code R), the alternative T allele encodes a stop codon (X). Hence, the S…

The allele associated with red hair and increased anesthetic response (when homozygous) is rs1805007(T); the wild-type, more common allele is rs1805007(C…

This SNP is 1 of 3 SNPs defining a haplotype that has been studied for association with eye color . The full details on the correspondence between the hap…

A SNP in rs1229984 encodes a form of the alcohol dehydrogenase ADH1B gene that significantly reduces the clearance rate of alcohol from the liver. This SN…

We are fast approaching an era in which genetic information is no longer exclusive or medicalized. Instead, as screening costs plummet and our knowledge …

Contents SNPedia is a Semantic MediaWiki-based wiki investigating human genetics. We keep track of all of the scientific literature known about each posi…

SNPedia (pronounced "snipedia") is a wiki-based bioinformatics web site that serves as a database of single nucleotide polymorphisms (SNPs). Each article…

Links to SNPedia Note: For some SNPs, testing providers detect the genotype from the opposite strand of DNA, so that the genotypes listed on openSNP don'…

Links to SNPedia Note: For some SNPs, testing providers detect the genotype from the opposite strand of DNA, so that the genotypes listed on openSNP don'…

Links to SNPedia Note: For some SNPs, testing providers detect the genotype from the opposite strand of DNA, so that the genotypes listed on openSNP don'…

Links to SNPedia Note: For some SNPs, testing providers detect the genotype from the opposite strand of DNA, so that the genotypes listed on openSNP don'…

Links to SNPedia Note: For some SNPs, testing providers detect the genotype from the opposite strand of DNA, so that the genotypes listed on openSNP don'…