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rs12350739

From SNPedia

Orientationplus
Stabilizedplus
Make rs12350739(A;A)
Make rs12350739(A;G)
Make rs12350739(G;G)
ReferenceGRCh38 38.1/141
Chromosome9
Position16885019
is asnp
is mentioned by
dbSNPrs12350739
ebirs12350739
HLIrs12350739
Exacrs12350739
Varsomers12350739
Maprs12350739
PheGenIrs12350739
hapmaprs12350739
1000 genomesrs12350739
hgdprs12350739
ensemblrs12350739
gopubmedrs12350739
geneviewrs12350739
scholarrs12350739
googlers12350739
pharmgkbrs12350739
gwascentralrs12350739
openSNPrs12350739
23andMers12350739
23andMe allrs12350739
SNP Nexus

SNPshotrs12350739
SNPdbers12350739
MSV3drs12350739
GWAS Ctlgrs12350739
Max Magnitude

[PMID 24916375] Human skin color is influenced by an intergenic DNA polymorphism regulating transcription of the nearby BNC2 pigmentation gene