rs28934272
From SNPedia
Merged into | rs121918166 |
Orientation | minus |
Stabilized | plus |
Make rs28934272(A;A) |
Make rs28934272(A;G) |
Make rs28934272(G;G) |
Reference | GRCh38 38.1/142 |
Chromosome | 15 |
Position | 27985101 |
Gene | OCA2 |
is a | snp |
is | mentioned by |
dbSNP | rs28934272 |
dbSNP (classic) | rs28934272 |
ClinGen | rs28934272 |
ebi | rs28934272 |
HLI | rs28934272 |
Exac | rs28934272 |
Gnomad | rs28934272 |
Varsome | rs28934272 |
LitVar | rs28934272 |
Map | rs28934272 |
PheGenI | rs28934272 |
Biobank | rs28934272 |
1000 genomes | rs28934272 |
hgdp | rs28934272 |
ensembl | rs28934272 |
geneview | rs28934272 |
scholar | rs28934272 |
rs28934272 | |
pharmgkb | rs28934272 |
gwascentral | rs28934272 |
openSNP | rs28934272 |
23andMe | rs28934272 |
SNPshot | rs28934272 |
SNPdbe | rs28934272 |
MSV3d | rs28934272 |
GWAS Ctlg | rs28934272 |
Status | Merged into rs121918166 |
Max Magnitude | 0 |
[PMID 17236130] A three-single-nucleotide polymorphism haplotype in intron 1 of OCA2 explains most human eye-color variation.