rs786201808
From SNPedia
Orientation | minus |
Stabilized | minus |
Geno | Mag | Summary |
---|---|---|
(A;G) | 6 | Ovarian cancer susceptibility |
(G;G) | 0 | common in clinvar |
Make rs786201808(A;A) |
Reference | GRCh38.p2 38.2/146 |
Chromosome | 17 |
Position | 61801388 |
Gene | BRIP1 |
is a | snp |
is | mentioned by |
dbSNP | rs786201808 |
dbSNP (classic) | rs786201808 |
ClinGen | rs786201808 |
ebi | rs786201808 |
HLI | rs786201808 |
Exac | rs786201808 |
Gnomad | rs786201808 |
Varsome | rs786201808 |
LitVar | rs786201808 |
Map | rs786201808 |
PheGenI | rs786201808 |
Biobank | rs786201808 |
1000 genomes | rs786201808 |
hgdp | rs786201808 |
ensembl | rs786201808 |
geneview | rs786201808 |
scholar | rs786201808 |
rs786201808 | |
pharmgkb | rs786201808 |
gwascentral | rs786201808 |
openSNP | rs786201808 |
23andMe | rs786201808 |
SNPshot | rs786201808 |
SNPdbe | rs786201808 |
MSV3d | rs786201808 |
GWAS Ctlg | rs786201808 |
Max Magnitude | 6 |
ClinVar | |
---|---|
Risk | rs786201808(A;A) |
Alt | rs786201808(A;A) |
Reference | Rs786201808(G;G) |
Significance | Pathogenic |
Disease | Hereditary cancer-predisposing syndrome |
Variation | info |
Gene | BRIP1 |
CLNDBN | Hereditary cancer-predisposing syndrome |
Reversed | 1 |
HGVS | NC_000017.10:g.59878749C>T |
CLNSRC | |
CLNACC | RCV000164287.1, |