rs587782848
From SNPedia
Orientation | minus |
Stabilized | minus |
Geno | Mag | Summary |
---|---|---|
(G;G) | 0 | common in clinvar |
Make rs587782848(A;A) |
Make rs587782848(A;G) |
Reference | GRCh38.p2 38.2/147 |
Chromosome | 17 |
Position | 35107376 |
Gene | RAD51D, RAD51L3-RFFL |
is a | snp |
is | mentioned by |
dbSNP | rs587782848 |
dbSNP (classic) | rs587782848 |
ClinGen | rs587782848 |
ebi | rs587782848 |
HLI | rs587782848 |
Exac | rs587782848 |
Gnomad | rs587782848 |
Varsome | rs587782848 |
LitVar | rs587782848 |
Map | rs587782848 |
PheGenI | rs587782848 |
Biobank | rs587782848 |
1000 genomes | rs587782848 |
hgdp | rs587782848 |
ensembl | rs587782848 |
geneview | rs587782848 |
scholar | rs587782848 |
rs587782848 | |
pharmgkb | rs587782848 |
gwascentral | rs587782848 |
openSNP | rs587782848 |
23andMe | rs587782848 |
SNPshot | rs587782848 |
SNPdbe | rs587782848 |
MSV3d | rs587782848 |
GWAS Ctlg | rs587782848 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs587782848(A;A) rs587782848(C;C) |
Alt | rs587782848(A;A) rs587782848(C;C) |
Reference | Rs587782848(G;G) |
Significance | Probable-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.33434395C>G; NC_000017.10:g.33434395C>T |
CLNSRC | |
CLNACC | RCV000223012.1, RCV000132446.2, RCV000476134.1, |