rs12350739
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs12350739(A;A) |
| Make rs12350739(A;G) |
| Make rs12350739(G;G) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 9 |
| Position | 16885019 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs12350739 |
| dbSNP (classic) | rs12350739 |
| ClinGen | rs12350739 |
| ebi | rs12350739 |
| HLI | rs12350739 |
| Exac | rs12350739 |
| Gnomad | rs12350739 |
| Varsome | rs12350739 |
| LitVar | rs12350739 |
| Map | rs12350739 |
| PheGenI | rs12350739 |
| Biobank | rs12350739 |
| 1000 genomes | rs12350739 |
| hgdp | rs12350739 |
| ensembl | rs12350739 |
| geneview | rs12350739 |
| scholar | rs12350739 |
| rs12350739 | |
| pharmgkb | rs12350739 |
| gwascentral | rs12350739 |
| openSNP | rs12350739 |
| 23andMe | rs12350739 |
| SNPshot | rs12350739 |
| SNPdbe | rs12350739 |
| MSV3d | rs12350739 |
| GWAS Ctlg | rs12350739 |
| Max Magnitude | 0 |
[PMID 24916375] Human skin color is influenced by an intergenic DNA polymorphism regulating transcription of the nearby BNC2 pigmentation gene
