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rs4778137

From SNPedia

Orientationplus
Stabilizedplus
Make rs4778137(C;C)
Make rs4778137(C;G)
Make rs4778137(G;G)
ReferenceGRCh38 38.1/141
Chromosome15
Position28082689
GeneOCA2
is asnp
is mentioned by
dbSNPrs4778137
ebirs4778137
HLIrs4778137
Exacrs4778137
Varsomers4778137
Maprs4778137
PheGenIrs4778137
hapmaprs4778137
1000 genomesrs4778137
hgdprs4778137
ensemblrs4778137
gopubmedrs4778137
geneviewrs4778137
scholarrs4778137
googlers4778137
pharmgkbrs4778137
gwascentralrs4778137
openSNPrs4778137
23andMers4778137
23andMe allrs4778137
SNP Nexus

SNPshotrs4778137
SNPdbers4778137
MSV3drs4778137
GWAS Ctlgrs4778137
GMAF0.4674
Max Magnitude
? (C;C) (C;G) (G;G) 28
[PMID 20308648OA-icon.png] Association Between a Germline OCA2 Polymorphism at Chromosome 15q13.1 and Estrogen Receptor-Negative Breast Cancer Survival

[PMID 17236130OA-icon.png] A three-single-nucleotide polymorphism haplotype in intron 1 of OCA2 explains most human eye-color variation.

[PMID 18252221OA-icon.png] Three genome-wide association studies and a linkage analysis identify HERC2 as a human iris color gene.