rs4911442
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Geno | Mag | Summary |
|---|---|---|
| (A;A) | 0 |
| Make rs4911442(A;G) |
| Make rs4911442(G;G) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 20 |
| Position | 34767243 |
| Gene | NCOA6 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs4911442 |
| dbSNP (classic) | rs4911442 |
| ClinGen | rs4911442 |
| ebi | rs4911442 |
| HLI | rs4911442 |
| Exac | rs4911442 |
| Gnomad | rs4911442 |
| Varsome | rs4911442 |
| LitVar | rs4911442 |
| Map | rs4911442 |
| PheGenI | rs4911442 |
| Biobank | rs4911442 |
| 1000 genomes | rs4911442 |
| hgdp | rs4911442 |
| ensembl | rs4911442 |
| geneview | rs4911442 |
| scholar | rs4911442 |
| rs4911442 | |
| pharmgkb | rs4911442 |
| gwascentral | rs4911442 |
| openSNP | rs4911442 |
| 23andMe | rs4911442 |
| SNPshot | rs4911442 |
| SNPdbe | rs4911442 |
| MSV3d | rs4911442 |
| GWAS Ctlg | rs4911442 |
| GMAF | 0.03949 |
| Max Magnitude | 0 |
| ? | (A;A) (A;G) (G;G) | 28 |
|---|---|---|
|
| ||
Influences appearance [1]
Digital Quantification of Human Eye Color Highlights Genetic Association of Three New Loci[2]
[PMID 18488026
] Common sequence variants on 20q11.22 confer melanoma susceptibility.
[PMID 19578364] Genome-wide association study identifies three loci associated with melanoma risk.
[PMID 20585627] Web-based, participant-driven studies yield novel genetic associations for common traits.
[PMID 23393597] Replication and Predictive Value of SNPs Associated with Melanoma and Pigmentation Traits in a Southern European Case-Control Study
[PMID 22628150] Variants at chromosome 20 (ASIP locus) and melanoma risk.
[PMID 25837821] Inherited genetic variants associated with occurrence of multiple primary melanoma
