rs730881942
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(G;G) | 0 | common in clinvar |
Make rs730881942(-;-) |
Make rs730881942(-;G) |
Reference | GRCh38.p2 38.2/144 |
Chromosome | 17 |
Position | 58692736 |
Gene | RAD51C, TEX14 |
is a | snp |
is | mentioned by |
dbSNP | rs730881942 |
dbSNP (classic) | rs730881942 |
ClinGen | rs730881942 |
ebi | rs730881942 |
HLI | rs730881942 |
Exac | rs730881942 |
Gnomad | rs730881942 |
Varsome | rs730881942 |
LitVar | rs730881942 |
Map | rs730881942 |
PheGenI | rs730881942 |
Biobank | rs730881942 |
1000 genomes | rs730881942 |
hgdp | rs730881942 |
ensembl | rs730881942 |
geneview | rs730881942 |
scholar | rs730881942 |
rs730881942 | |
pharmgkb | rs730881942 |
gwascentral | rs730881942 |
openSNP | rs730881942 |
23andMe | rs730881942 |
SNPshot | rs730881942 |
SNPdbe | rs730881942 |
MSV3d | rs730881942 |
GWAS Ctlg | rs730881942 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs730881942(-;-) |
Alt | rs730881942(-;-) |
Reference | Rs730881942(G;G) |
Significance | Other |
Disease | Breast-ovarian cancer Hereditary cancer-predisposing syndrome Fanconi anemia not provided |
Variation | info |
Gene | TEX14 RAD51C |
CLNDBN | Breast-ovarian cancer, familial 3 Hereditary cancer-predisposing syndrome Fanconi anemia, complementation group O not provided |
Reversed | 0 |
HGVS | NC_000017.10:g.56770097delG |
CLNSRC | OMIM Allelic Variant |
CLNACC | RCV000024266.3, RCV000160936.3, RCV000205375.2, RCV000212931.1, |