rs786202788
From SNPedia
Orientation | minus |
Stabilized | minus |
Geno | Mag | Summary |
---|---|---|
(A;G) | 6 | Ovarian cancer susceptibility |
(G;G) | 0 | common in clinvar |
(G;T) | 6 | Ovarian cancer susceptibility |
Make rs786202788(A;A) |
Reference | GRCh38.p2 38.2/146 |
Chromosome | 17 |
Position | 35119531 |
Gene | RAD51D, RAD51L3-RFFL |
is a | snp |
is | mentioned by |
dbSNP | rs786202788 |
dbSNP (classic) | rs786202788 |
ClinGen | rs786202788 |
ebi | rs786202788 |
HLI | rs786202788 |
Exac | rs786202788 |
Gnomad | rs786202788 |
Varsome | rs786202788 |
LitVar | rs786202788 |
Map | rs786202788 |
PheGenI | rs786202788 |
Biobank | rs786202788 |
1000 genomes | rs786202788 |
hgdp | rs786202788 |
ensembl | rs786202788 |
geneview | rs786202788 |
scholar | rs786202788 |
rs786202788 | |
pharmgkb | rs786202788 |
gwascentral | rs786202788 |
openSNP | rs786202788 |
23andMe | rs786202788 |
SNPshot | rs786202788 |
SNPdbe | rs786202788 |
MSV3d | rs786202788 |
GWAS Ctlg | rs786202788 |
Max Magnitude | 6 |
ClinVar | |
---|---|
Risk | rs786202788(A;A) |
Alt | rs786202788(A;A) |
Reference | Rs786202788(G;G) |
Significance | Probable-Pathogenic |
Disease | Hereditary cancer-predisposing syndrome |
Variation | info |
Gene | RAD51D RAD51L3-RFFL |
CLNDBN | Hereditary cancer-predisposing syndrome |
Reversed | 1 |
HGVS | NC_000017.10:g.33446550C>T |
CLNSRC | |
CLNACC | RCV000165776.1, |