rs4636294
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs4636294(A;A) |
| Make rs4636294(A;G) |
| Make rs4636294(G;G) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 9 |
| Position | 21747804 |
| Gene | LOC107987026 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs4636294 |
| dbSNP (classic) | rs4636294 |
| ClinGen | rs4636294 |
| ebi | rs4636294 |
| HLI | rs4636294 |
| Exac | rs4636294 |
| Gnomad | rs4636294 |
| Varsome | rs4636294 |
| LitVar | rs4636294 |
| Map | rs4636294 |
| PheGenI | rs4636294 |
| Biobank | rs4636294 |
| 1000 genomes | rs4636294 |
| hgdp | rs4636294 |
| ensembl | rs4636294 |
| geneview | rs4636294 |
| scholar | rs4636294 |
| rs4636294 | |
| pharmgkb | rs4636294 |
| gwascentral | rs4636294 |
| openSNP | rs4636294 |
| 23andMe | rs4636294 |
| SNPshot | rs4636294 |
| SNPdbe | rs4636294 |
| MSV3d | rs4636294 |
| GWAS Ctlg | rs4636294 |
| GMAF | 0.3751 |
| Max Magnitude | 0 |
| ? | (A;A) (A;G) (G;G) | 28 |
|---|---|---|
|
| ||
| GWAS snp | |
|---|---|
| PMID | [PMID 19578365 ]
|
| Trait | Cutaneous nevi |
| Title | Genome-wide association study identifies variants at 9p21 and 22q13 associated with development of cutaneous nevi |
| Risk Allele | A |
| P-val | 3E-15 |
| Odds Ratio | 0.20 [0.13-0.27] increase in log nevus count |
[PMID 19578364] Genome-wide association study identifies three loci associated with melanoma risk.
[PMID 19686382] Genome-wide associations studies for melanoma and nevi.
[PMID 30680790] Phenotypic and Genotypic Analysis of Amelanotic and Hypomelanotic Melanoma Patients.
