rs587782695
From SNPedia
Orientation | minus |
Stabilized | minus |
Geno | Mag | Summary |
---|---|---|
(C;C) | 0 | common in clinvar |
(C;T) | 6 | Ovarian cancer susceptibility |
Make rs587782695(T;T) |
Reference | GRCh38.p2 38.2/144 |
Chromosome | 17 |
Position | 35106415 |
Gene | RAD51D, RAD51L3-RFFL |
is a | snp |
is | mentioned by |
dbSNP | rs587782695 |
dbSNP (classic) | rs587782695 |
ClinGen | rs587782695 |
ebi | rs587782695 |
HLI | rs587782695 |
Exac | rs587782695 |
Gnomad | rs587782695 |
Varsome | rs587782695 |
LitVar | rs587782695 |
Map | rs587782695 |
PheGenI | rs587782695 |
Biobank | rs587782695 |
1000 genomes | rs587782695 |
hgdp | rs587782695 |
ensembl | rs587782695 |
geneview | rs587782695 |
scholar | rs587782695 |
rs587782695 | |
pharmgkb | rs587782695 |
gwascentral | rs587782695 |
openSNP | rs587782695 |
23andMe | rs587782695 |
SNPshot | rs587782695 |
SNPdbe | rs587782695 |
MSV3d | rs587782695 |
GWAS Ctlg | rs587782695 |
Max Magnitude | 6 |
ClinVar | |
---|---|
Risk | rs587782695(T;T) |
Alt | rs587782695(T;T) |
Reference | Rs587782695(C;C) |
Significance | Pathogenic |
Disease | Hereditary cancer-predisposing syndrome Breast-ovarian cancer |
Variation | info |
Gene | RAD51D RAD51L3-RFFL |
CLNDBN | Hereditary cancer-predisposing syndrome Breast-ovarian cancer, familial 4 |
Reversed | 1 |
HGVS | NC_000017.10:g.33433434G>A |
CLNSRC | |
CLNACC | RCV000132135.3, RCV000464954.1, |