rs786202750
From SNPedia
Orientation | minus |
Stabilized | minus |
Geno | Mag | Summary |
---|---|---|
(-;T) | 6 | Ovarian cancer susceptibility |
(T;T) | 0 | common in clinvar |
Make rs786202750(-;-) |
Reference | GRCh38.p2 38.2/146 |
Chromosome | 17 |
Position | 35106398 |
Gene | RAD51D, RAD51L3-RFFL |
is a | snp |
is | mentioned by |
dbSNP | rs786202750 |
dbSNP (classic) | rs786202750 |
ClinGen | rs786202750 |
ebi | rs786202750 |
HLI | rs786202750 |
Exac | rs786202750 |
Gnomad | rs786202750 |
Varsome | rs786202750 |
LitVar | rs786202750 |
Map | rs786202750 |
PheGenI | rs786202750 |
Biobank | rs786202750 |
1000 genomes | rs786202750 |
hgdp | rs786202750 |
ensembl | rs786202750 |
geneview | rs786202750 |
scholar | rs786202750 |
rs786202750 | |
pharmgkb | rs786202750 |
gwascentral | rs786202750 |
openSNP | rs786202750 |
23andMe | rs786202750 |
SNPshot | rs786202750 |
SNPdbe | rs786202750 |
MSV3d | rs786202750 |
GWAS Ctlg | rs786202750 |
Max Magnitude | 6 |
ClinVar | |
---|---|
Risk | rs786202750(-;-) |
Alt | rs786202750(-;-) |
Reference | Rs786202750(T;T) |
Significance | Pathogenic |
Disease | Hereditary cancer-predisposing syndrome |
Variation | info |
Gene | RAD51D RAD51L3-RFFL |
CLNDBN | Hereditary cancer-predisposing syndrome |
Reversed | 1 |
HGVS | NC_000017.10:g.33433417delA |
CLNSRC | |
CLNACC | RCV000165722.1, |