rs761564262
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs761564262(C;C) |
| Make rs761564262(C;G) |
| Make rs761564262(G;G) |
| Reference | GRCh38.p7 38.3/151 |
| Chromosome | 19 |
| Position | 43546884 |
| Gene | XRCC1 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs761564262 |
| dbSNP (classic) | rs761564262 |
| ClinGen | rs761564262 |
| ebi | rs761564262 |
| HLI | rs761564262 |
| Exac | rs761564262 |
| Gnomad | rs761564262 |
| Varsome | rs761564262 |
| LitVar | rs761564262 |
| Map | rs761564262 |
| PheGenI | rs761564262 |
| Biobank | rs761564262 |
| 1000 genomes | rs761564262 |
| hgdp | rs761564262 |
| ensembl | rs761564262 |
| geneview | rs761564262 |
| scholar | rs761564262 |
| rs761564262 | |
| pharmgkb | rs761564262 |
| gwascentral | rs761564262 |
| openSNP | rs761564262 |
| 23andMe | rs761564262 |
| SNPshot | rs761564262 |
| SNPdbe | rs761564262 |
| MSV3d | rs761564262 |
| GWAS Ctlg | rs761564262 |
| Max Magnitude | 0 |
aka NM_006297.2(XRCC1):c.1293G>C or (p.Lys431Asn)
OMIM pathogenic variant
