rs587782528
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(C;C) | 0 | common in clinvar |
Make rs587782528(C;T) |
Make rs587782528(T;T) |
Reference | GRCh38.p2 38.2/144 |
Chromosome | 17 |
Position | 58692740 |
Gene | RAD51C, TEX14 |
is a | snp |
is | mentioned by |
dbSNP | rs587782528 |
dbSNP (classic) | rs587782528 |
ClinGen | rs587782528 |
ebi | rs587782528 |
HLI | rs587782528 |
Exac | rs587782528 |
Gnomad | rs587782528 |
Varsome | rs587782528 |
LitVar | rs587782528 |
Map | rs587782528 |
PheGenI | rs587782528 |
Biobank | rs587782528 |
1000 genomes | rs587782528 |
hgdp | rs587782528 |
ensembl | rs587782528 |
geneview | rs587782528 |
scholar | rs587782528 |
rs587782528 | |
pharmgkb | rs587782528 |
gwascentral | rs587782528 |
openSNP | rs587782528 |
23andMe | rs587782528 |
SNPshot | rs587782528 |
SNPdbe | rs587782528 |
MSV3d | rs587782528 |
GWAS Ctlg | rs587782528 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs587782528(T;T) |
Alt | rs587782528(T;T) |
Reference | Rs587782528(C;C) |
Significance | Pathogenic |
Disease | Hereditary cancer-predisposing syndrome Fanconi anemia not provided Breast-ovarian cancer |
Variation | info |
Gene | TEX14 RAD51C |
CLNDBN | Hereditary cancer-predisposing syndrome Fanconi anemia, complementation group O not provided Breast-ovarian cancer, familial 3 |
Reversed | 0 |
HGVS | NC_000017.10:g.56770101C>T |
CLNSRC | |
CLNACC | RCV000131716.4, RCV000196217.2, RCV000212932.1, RCV000410098.1, |