rs12913832
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(A;A) | 0 | brown eye color, 80% of the time |
(A;G) | brown eye color | |
(G;G) | 2.5 | blue eye color, 99% of the time |
Reference | GRCh38 38.1/141 |
Chromosome | 15 |
Position | 28120472 |
Gene | HERC2 |
is a | snp |
is | mentioned by |
dbSNP | rs12913832 |
dbSNP (classic) | rs12913832 |
ClinGen | rs12913832 |
ebi | rs12913832 |
HLI | rs12913832 |
Exac | rs12913832 |
Gnomad | rs12913832 |
Varsome | rs12913832 |
LitVar | rs12913832 |
Map | rs12913832 |
PheGenI | rs12913832 |
Biobank | rs12913832 |
1000 genomes | rs12913832 |
hgdp | rs12913832 |
ensembl | rs12913832 |
geneview | rs12913832 |
scholar | rs12913832 |
rs12913832 | |
pharmgkb | rs12913832 |
gwascentral | rs12913832 |
openSNP | rs12913832 |
23andMe | rs12913832 |
SNPshot | rs12913832 |
SNPdbe | rs12913832 |
MSV3d | rs12913832 |
GWAS Ctlg | rs12913832 |
GMAF | 0.2911 |
Max Magnitude | 2.5 |
? | (A;A) (A;G) (G;G) | 28 |
---|---|---|
|
rs12913832 is a SNP near the OCA2 gene that may be functionally linked to blue or brown eye color, due to a lowering of promoter activity of the OCA2 gene. Blue eye color is associated with the rs12913832(G;G) genotype.[PMID 18172690, PMID 18252222]
For green versus blue eye color rs12913832 in OCA2/HERC2 has a score of 51.5 and an estimated allelic OR of 8.43 . The SNP rs1667394 in this same region has an estimated OR of (4.85–10.06).10.1371/journal.pgen.1000993
rs12913832 is also part of a haplotype spanning 166kB on chromosome 15, defined by 13 SNPs listed below, that is found in 97% of all Caucasians with blue eyes. In this haplotype, variations in rs1129038 and rs12913832 are relatively common in Caucasians though rare among other racial groups.[PMID 18172690]
[PMID 18650849] rs12913832-T (brown eye) homozygotes compared to rs12913832-C (blue eye). correlations with skin, eye, and hair color variation.
The "h-1" haplotype found in homozygous state in 97% of individuals with blue eye color is composed as follows [PMID 18172690]:
rs4778241(C)
rs1129038(A)
rs12593929(A)
rs12913832(G)
rs7183877(C)
rs3935591(G)
rs7170852(A)
rs2238289(T)
rs3940272(C)
rs8028689(T)
rs2240203(A)
rs11631797(G)
rs916977(G)
blog coverage
10.1038/ncomms10815 A genome-wide association scan in admixed Latin Americans identifies loci influencing facial and scalp hair features
GWAS | |
---|---|
SNP | rs12913832 |
PubMedID | [PMID 18483556] |
Condition | Black vs. red hair color |
Gene | HERC2 |
Risk Allele | A |
pValue | 1.00E-077 |
OR | 0.44 |
95% CI | 0.40-0.48) decrease in hair color scor |
[PMID 19278018] Brief communication: Blue eyes in lemurs and humans: Same phenotype, different genetic mechanism
[PMID 19208107] Interactions between HERC2, OCA2 and MC1R may influence human pigmentation phenotype.
GWAS snp | |
---|---|
PMID | [PMID 20463881] |
Trait | Eye color traits |
Title | Digital quantification of human eye color highlights genetic association of three new loci |
Risk Allele | |
P-val | 0 |
Odds Ratio | None None |
GWAS snp | |
---|---|
PMID | [PMID 20585627] |
Trait | Eye color |
Title | Web-based, participant-driven studies yield novel genetic associations for common traits |
Risk Allele | A |
P-val | 3E-52 |
Odds Ratio | 8.43 [NR] |
[PMID 20457063] Human eye colour and HERC2, OCA2 and MATP
[PMID 22615734] The Classical Pink-Eyed Dilution Mutation Affects Angiogenic Responsiveness
[PMID 22234890] HERC2 rs12913832 modulates human pigmentation by attenuating chromatin-loop formation between a long-range enhancer and the OCA2 promoter.
[PMID 19340012] Genome-wide association study of tanning phenotype in a population of European ancestry.
[PMID 19472299] Genotyping of five single nucleotide polymorphisms in the OCA2 and HERC2 genes associated with blue-brown eye color in the Japanese population.
[PMID 19619260] Genetics of human iris colour and patterns.
[PMID 19668368] Ancestry analysis in the 11-M Madrid bomb attack investigation.
[PMID 19711812] [Genetic analysis of the putative remains of general Wladyslaw Sikorski].
[PMID 20018053] A genome-wide association scan for rheumatoid arthritis data by Hotelling's T2 tests.
[PMID 20221248] Association of the OCA2 polymorphism His615Arg with melanin content in east Asian populations: further evidence of convergent evolution of skin pigmentation.
[PMID 20569440] Alterations in LMTK2, MSMB and HNF1B gene expression are associated with the development of prostate cancer.
[PMID 20629734] Genetic analysis of three important genes in pigmentation and melanoma susceptibility: CDKN2A, MC1R and HERC2/OCA2.
[PMID 21253569] Genome-wide association study SNPs in the human genome diversity project populations: does selection affect unlinked SNPs with shared trait associations?
[PMID 21926416] Genome-wide association study identifies novel loci predisposing to cutaneous melanoma.
[PMID 22101828] Technical note: quantitative measures of iris color using high resolution photographs.
[PMID 23100201] A single-nucleotide polymorphism (SNP) multiplex system: the association of five SNPs with human eye and hair color in the Slovenian population and comparison using a Bayesian network and logistic regression model
[PMID 23548203] Genome-wide association studies identify several new loci associated with pigmentation traits and skin cancer risk in European Americans
[PMID 22709892] Further development of forensic eye color predictive tests.
[PMID 23543094] Testing for associations between loci and environmental gradients using latent factor mixed models.
[PMID 23771755] Improved eye- and skin-color prediction based on 8 SNPs.
ClinVar | |
---|---|
Risk | Rs12913832(G;G) |
Alt | Rs12913832(G;G) |
Reference | Rs12913832(A;A) |
Significance | Other |
Disease | Skin/hair/eye pigmentation |
Variation | info |
Gene | HERC2 |
CLNDBN | Skin/hair/eye pigmentation, variation in, 1 |
Reversed | 0 |
HGVS | NC_000015.9:g.28365618A>G |
CLNSRC | OMIM Allelic Variant |
CLNACC | RCV000005011.3, |
[PMID 28242083] Association of five SNPs with human hair colour in the Polish population.
- Is a snp
- In dbSNP
- SNPs on chromosome 15
- Has genotype
- Has population
- Uses doi
- GWAS
- Uses omim
- On chip 23andMe v1
- On chip 23andMe v2
- On chip 23andMe v3
- On chip 23andMe v4
- On chip 23andMe v5
- On chip Affy GenomeWide 6
- On chip Ancestry v2
- On chip HumanOmni1Quad
- On chip Illumina Human 1M
- On chip Ancestry v2c
- On chip Ancestry v2d
- Pages using PMID magic links