rs754367349
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Geno | Mag | Summary |
|---|---|---|
| (T;T) | 0 | common in clinvar |
| Make rs754367349(-;-) |
| Make rs754367349(-;T) |
| Reference | GRCh38.p7 38.3/150 |
| Chromosome | 17 |
| Position | 58709927 |
| Gene | RAD51C |
| is a | snp |
| is | mentioned by |
| dbSNP | rs754367349 |
| dbSNP (classic) | rs754367349 |
| ClinGen | rs754367349 |
| ebi | rs754367349 |
| HLI | rs754367349 |
| Exac | rs754367349 |
| Gnomad | rs754367349 |
| Varsome | rs754367349 |
| LitVar | rs754367349 |
| Map | rs754367349 |
| PheGenI | rs754367349 |
| Biobank | rs754367349 |
| 1000 genomes | rs754367349 |
| hgdp | rs754367349 |
| ensembl | rs754367349 |
| geneview | rs754367349 |
| scholar | rs754367349 |
| rs754367349 | |
| pharmgkb | rs754367349 |
| gwascentral | rs754367349 |
| openSNP | rs754367349 |
| 23andMe | rs754367349 |
| SNPshot | rs754367349 |
| SNPdbe | rs754367349 |
| MSV3d | rs754367349 |
| GWAS Ctlg | rs754367349 |
| Max Magnitude | 0 |
| ClinVar | |
|---|---|
| Risk | rs754367349(-;-) |
| Alt | rs754367349(-;-) |
| Reference | Rs754367349(T;T) |
| Significance | Pathogenic |
| Disease | not provided |
| Variation | info |
| Gene | RAD51C |
| CLNDBN | not provided |
| Reversed | 0 |
| HGVS | NC_000017.10:g.56787288delT |
| CLNSRC | |
| CLNACC | RCV000484016.1, |
