rs6058017
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Geno | Mag | Summary |
|---|---|---|
| (A;A) | 0 | common in clinvar |
| Make rs6058017(A;G) |
| Make rs6058017(G;G) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 20 |
| Position | 34269192 |
| Gene | AHCY, ASIP |
| is a | snp |
| is | mentioned by |
| dbSNP | rs6058017 |
| dbSNP (classic) | rs6058017 |
| ClinGen | rs6058017 |
| ebi | rs6058017 |
| HLI | rs6058017 |
| Exac | rs6058017 |
| Gnomad | rs6058017 |
| Varsome | rs6058017 |
| LitVar | rs6058017 |
| Map | rs6058017 |
| PheGenI | rs6058017 |
| Biobank | rs6058017 |
| 1000 genomes | rs6058017 |
| hgdp | rs6058017 |
| ensembl | rs6058017 |
| geneview | rs6058017 |
| scholar | rs6058017 |
| rs6058017 | |
| pharmgkb | rs6058017 |
| gwascentral | rs6058017 |
| openSNP | rs6058017 |
| 23andMe | rs6058017 |
| SNPshot | rs6058017 |
| SNPdbe | rs6058017 |
| MSV3d | rs6058017 |
| GWAS Ctlg | rs6058017 |
| GMAF | 0.2893 |
| Max Magnitude | 0 |
Influences appearance gnxp
[PMID 17999355
] A genomewide association study of skin pigmentation in a South Asian population.
[PMID 19384953] Genetic variants in pigmentation genes, pigmentary phenotypes, and risk of skin cancer in Caucasians.
[PMID 19995372] Melanoma susceptibility variants on chromosome 20q11.22 are associated with pigmentary traits and the risk of nonmelanoma skin cancer.
| ClinVar | |
|---|---|
| Risk | rs6058017(G;G) |
| Alt | rs6058017(G;G) |
| Reference | Rs6058017(A;A) |
| Significance | Other |
| Disease | Skin/hair/eye pigmentation |
| Variation | info |
| Gene | ASIP |
| CLNDBN | Skin/hair/eye pigmentation, variation in, 9 |
| Reversed | 0 |
| HGVS | NC_000020.10:g.32856998A>G |
| CLNSRC | OMIM Allelic Variant |
| CLNACC | RCV000009892.5, |
