rs150855676
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Geno | Mag | Summary |
|---|---|---|
| (G;G) | 0 | common in clinvar |
| Make rs150855676(A;A) |
| Make rs150855676(A;G) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 1 |
| Position | 6112171 |
| Gene | CHD5 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs150855676 |
| dbSNP (classic) | rs150855676 |
| ClinGen | rs150855676 |
| ebi | rs150855676 |
| HLI | rs150855676 |
| Exac | rs150855676 |
| Gnomad | rs150855676 |
| Varsome | rs150855676 |
| LitVar | rs150855676 |
| Map | rs150855676 |
| PheGenI | rs150855676 |
| Biobank | rs150855676 |
| 1000 genomes | rs150855676 |
| hgdp | rs150855676 |
| ensembl | rs150855676 |
| geneview | rs150855676 |
| scholar | rs150855676 |
| rs150855676 | |
| pharmgkb | rs150855676 |
| gwascentral | rs150855676 |
| openSNP | rs150855676 |
| 23andMe | rs150855676 |
| SNPshot | rs150855676 |
| SNPdbe | rs150855676 |
| MSV3d | rs150855676 |
| GWAS Ctlg | rs150855676 |
| Max Magnitude | 0 |
| ClinVar | |
|---|---|
| Risk | rs150855676(A;A) |
| Alt | rs150855676(A;A) |
| Reference | Rs150855676(G;G) |
| Significance | Untested |
| Disease | Malignant melanoma |
| Variation | info |
| Gene | CHD5 |
| CLNDBN | Malignant melanoma |
| Reversed | 0 |
| HGVS | NC_000001.11:g.6112171G>A |
| CLNSRC | ClinVar |
| CLNACC | RCV000060228.2, |
[PMID 21499247
] Exome sequencing identifies GRIN2A as frequently mutated in melanoma.
