rs757128712
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs757128712(A;A) |
| Make rs757128712(A;G) |
| Reference | GRCh38.p2 38.2/147 |
| Chromosome | 17 |
| Position | 58692789 |
| Gene | RAD51C, TEX14 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs757128712 |
| dbSNP (classic) | rs757128712 |
| ClinGen | rs757128712 |
| ebi | rs757128712 |
| HLI | rs757128712 |
| Exac | rs757128712 |
| Gnomad | rs757128712 |
| Varsome | rs757128712 |
| LitVar | rs757128712 |
| Map | rs757128712 |
| PheGenI | rs757128712 |
| Biobank | rs757128712 |
| 1000 genomes | rs757128712 |
| hgdp | rs757128712 |
| ensembl | rs757128712 |
| geneview | rs757128712 |
| scholar | rs757128712 |
| rs757128712 | |
| pharmgkb | rs757128712 |
| gwascentral | rs757128712 |
| openSNP | rs757128712 |
| 23andMe | rs757128712 |
| SNPshot | rs757128712 |
| SNPdbe | rs757128712 |
| MSV3d | rs757128712 |
| GWAS Ctlg | rs757128712 |
| Max Magnitude | 0 |
| ClinVar | |
|---|---|
| Risk | rs757128712(A;A) rs757128712(T;T) |
| Alt | rs757128712(A;A) rs757128712(T;T) |
| Reference | Rs757128712(G;G) |
| Significance | Pathogenic |
| Disease | Hereditary cancer-predisposing syndrome not provided |
| Variation | info |
| Gene | TEX14 RAD51C |
| CLNDBN | Hereditary cancer-predisposing syndrome not provided |
| Reversed | 0 |
| HGVS | NC_000017.10:g.56770150G>T |
| CLNSRC | |
| CLNACC | RCV000216860.1, RCV000479141.1, |
