rs193302997
From SNPedia
| Orientation | minus |
| Stabilized | minus |
| Geno | Mag | Summary |
|---|---|---|
| (A;A) | 0 | common in clinvar |
| Make rs193302997(C;C) |
| Make rs193302997(C;T) |
| Make rs193302997(T;T) |
| Reference | GRCh38.p7 38.3/150 |
| Chromosome | MT |
| Position | 15670 |
| Gene | CYTB |
| is a | snp |
| is | mentioned by |
| dbSNP | rs193302997 |
| dbSNP (classic) | rs193302997 |
| ClinGen | rs193302997 |
| ebi | rs193302997 |
| HLI | rs193302997 |
| Exac | rs193302997 |
| Gnomad | rs193302997 |
| Varsome | rs193302997 |
| LitVar | rs193302997 |
| Map | rs193302997 |
| PheGenI | rs193302997 |
| Biobank | rs193302997 |
| 1000 genomes | rs193302997 |
| hgdp | rs193302997 |
| ensembl | rs193302997 |
| geneview | rs193302997 |
| scholar | rs193302997 |
| rs193302997 | |
| pharmgkb | rs193302997 |
| gwascentral | rs193302997 |
| openSNP | rs193302997 |
| 23andMe | rs193302997 |
| SNPshot | rs193302997 |
| SNPdbe | rs193302997 |
| MSV3d | rs193302997 |
| GWAS Ctlg | rs193302997 |
| Max Magnitude | 0 |
| ClinVar | |
|---|---|
| Risk | rs193302997(C;C) rs193302997(G;G) rs193302997(T;T) |
| Alt | rs193302997(C;C) rs193302997(G;G) rs193302997(T;T) |
| Reference | Rs193302997(A;A) |
| Significance | Probable-Pathogenic |
| Disease | Neoplasm of ovary |
| Variation | info |
| Gene | CYTB |
| CLNDBN | Neoplasm of ovary |
| Reversed | 1 |
| HGVS | NC_012920.1:m.15670T>C |
| CLNSRC | |
| CLNACC | RCV000133458.1, |
