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rs7170989

From SNPedia

Orientationplus
Stabilizedplus
Make rs7170989(C;C)
Make rs7170989(C;T)
Make rs7170989(T;T)
ReferenceGRCh38 38.1/141
Chromosome15
Position27955262
GeneOCA2
is asnp
is mentioned by
dbSNPrs7170989
ebirs7170989
HLIrs7170989
Exacrs7170989
Varsomers7170989
Maprs7170989
PheGenIrs7170989
hapmaprs7170989
1000 genomesrs7170989
hgdprs7170989
ensemblrs7170989
gopubmedrs7170989
geneviewrs7170989
scholarrs7170989
googlers7170989
pharmgkbrs7170989
gwascentralrs7170989
openSNPrs7170989
23andMers7170989
23andMe allrs7170989
SNP Nexus

SNPshotrs7170989
SNPdbers7170989
MSV3drs7170989
GWAS Ctlgrs7170989
GMAF0.449
Max Magnitude
? (C;C) (C;T) (T;T) 28
[PMID 23100201OA-icon.png] 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 17236130OA-icon.png] A three-single-nucleotide polymorphism haplotype in intron 1 of OCA2 explains most human eye-color variation.


[PMID 17999355OA-icon.png] A genomewide association study of skin pigmentation in a South Asian population.