rs7170989
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs7170989(C;C) |
Make rs7170989(C;T) |
Make rs7170989(T;T) |
Reference | GRCh38 38.1/141 |
Chromosome | 15 |
Position | 27955262 |
Gene | OCA2 |
is a | snp |
is | mentioned by |
dbSNP | rs7170989 |
dbSNP (classic) | rs7170989 |
ClinGen | rs7170989 |
ebi | rs7170989 |
HLI | rs7170989 |
Exac | rs7170989 |
Gnomad | rs7170989 |
Varsome | rs7170989 |
LitVar | rs7170989 |
Map | rs7170989 |
PheGenI | rs7170989 |
Biobank | rs7170989 |
1000 genomes | rs7170989 |
hgdp | rs7170989 |
ensembl | rs7170989 |
geneview | rs7170989 |
scholar | rs7170989 |
rs7170989 | |
pharmgkb | rs7170989 |
gwascentral | rs7170989 |
openSNP | rs7170989 |
23andMe | rs7170989 |
SNPshot | rs7170989 |
SNPdbe | rs7170989 |
MSV3d | rs7170989 |
GWAS Ctlg | rs7170989 |
GMAF | 0.449 |
Max Magnitude | 0 |
? | (C;C) (C;T) (T;T) | 28 |
---|---|---|
|
[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 17236130] A three-single-nucleotide polymorphism haplotype in intron 1 of OCA2 explains most human eye-color variation.
[PMID 17999355] A genomewide association study of skin pigmentation in a South Asian population.