rs773906955
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(A;G) | 6 | Ovarian cancer susceptibility |
(G;G) | 0 | common in clinvar |
Make rs773906955(A;A) |
Reference | GRCh38.p2 38.2/147 |
Chromosome | 17 |
Position | 35107026 |
Gene | RAD51D, RAD51L3-RFFL |
is a | snp |
is | mentioned by |
dbSNP | rs773906955 |
dbSNP (classic) | rs773906955 |
ClinGen | rs773906955 |
ebi | rs773906955 |
HLI | rs773906955 |
Exac | rs773906955 |
Gnomad | rs773906955 |
Varsome | rs773906955 |
LitVar | rs773906955 |
Map | rs773906955 |
PheGenI | rs773906955 |
Biobank | rs773906955 |
1000 genomes | rs773906955 |
hgdp | rs773906955 |
ensembl | rs773906955 |
geneview | rs773906955 |
scholar | rs773906955 |
rs773906955 | |
pharmgkb | rs773906955 |
gwascentral | rs773906955 |
openSNP | rs773906955 |
23andMe | rs773906955 |
SNPshot | rs773906955 |
SNPdbe | rs773906955 |
MSV3d | rs773906955 |
GWAS Ctlg | rs773906955 |
Max Magnitude | 6 |
ClinVar | |
---|---|
Risk | rs773906955(A;A) |
Alt | rs773906955(A;A) |
Reference | Rs773906955(G;G) |
Significance | Pathogenic |
Disease | Hereditary cancer-predisposing syndrome |
Variation | info |
Gene | RAD51D RAD51L3-RFFL |
CLNDBN | Hereditary cancer-predisposing syndrome |
Reversed | 0 |
HGVS | NC_000017.10:g.33434045G>A |
CLNSRC | |
CLNACC | RCV000215616.1, |