rs201940931
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Geno | Mag | Summary |
|---|---|---|
| (T;T) | 0 | common in clinvar |
| Make rs201940931(G;G) |
| Make rs201940931(G;T) |
| Reference | GRCh38.p2 38.2/144 |
| Chromosome | 3 |
| Position | 14165587 |
| Gene | XPC |
| is a | snp |
| is | mentioned by |
| dbSNP | rs201940931 |
| dbSNP (classic) | rs201940931 |
| ClinGen | rs201940931 |
| ebi | rs201940931 |
| HLI | rs201940931 |
| Exac | rs201940931 |
| Gnomad | rs201940931 |
| Varsome | rs201940931 |
| LitVar | rs201940931 |
| Map | rs201940931 |
| PheGenI | rs201940931 |
| Biobank | rs201940931 |
| 1000 genomes | rs201940931 |
| hgdp | rs201940931 |
| ensembl | rs201940931 |
| geneview | rs201940931 |
| scholar | rs201940931 |
| rs201940931 | |
| pharmgkb | rs201940931 |
| gwascentral | rs201940931 |
| openSNP | rs201940931 |
| 23andMe | rs201940931 |
| SNPshot | rs201940931 |
| SNPdbe | rs201940931 |
| MSV3d | rs201940931 |
| GWAS Ctlg | rs201940931 |
| Max Magnitude | 0 |
| ClinVar | |
|---|---|
| Risk | rs201940931(G;G) |
| Alt | rs201940931(G;G) |
| Reference | Rs201940931(T;T) |
| Significance | Pathogenic |
| Disease | Xeroderma pigmentosum |
| Variation | info |
| Gene | XPC |
| CLNDBN | Xeroderma pigmentosum, group C |
| Reversed | 0 |
| HGVS | NC_000003.11:g.14207087T>G |
| CLNSRC | |
| CLNACC | RCV000170430.1, |
