rs786202179
From SNPedia
Orientation | minus |
Stabilized | minus |
Geno | Mag | Summary |
---|---|---|
(-;CGGCTTTCCCCGTGAA) | 6 | Ovarian cancer susceptibility |
(CGGCTTTCCCCGTGAA;CGGCTTTCCCCGTGAA) | 0 | common in clinvar |
Make rs786202179(-;-) |
Reference | GRCh38.p2 38.2/146 |
Chromosome | 17 |
Position | 35118564 |
Gene | RAD51D, RAD51L3-RFFL |
is a | snp |
is | mentioned by |
dbSNP | rs786202179 |
dbSNP (classic) | rs786202179 |
ClinGen | rs786202179 |
ebi | rs786202179 |
HLI | rs786202179 |
Exac | rs786202179 |
Gnomad | rs786202179 |
Varsome | rs786202179 |
LitVar | rs786202179 |
Map | rs786202179 |
PheGenI | rs786202179 |
Biobank | rs786202179 |
1000 genomes | rs786202179 |
hgdp | rs786202179 |
ensembl | rs786202179 |
geneview | rs786202179 |
scholar | rs786202179 |
rs786202179 | |
pharmgkb | rs786202179 |
gwascentral | rs786202179 |
openSNP | rs786202179 |
23andMe | rs786202179 |
SNPshot | rs786202179 |
SNPdbe | rs786202179 |
MSV3d | rs786202179 |
GWAS Ctlg | rs786202179 |
Max Magnitude | 6 |
ClinVar | |
---|---|
Risk | rs786202179(-;-) |
Alt | rs786202179(-;-) |
Reference | Rs786202179(CGGCTTTCCCCGTGAA;CGGCTTTCCCCGTGAA) |
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.33445583_33445598del16 |
CLNSRC | |
CLNACC | RCV000164875.1, |