rs771654971
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(-;-) | 0 | common in clinvar |
(-;T) | 6 | Ovarian cancer susceptibility |
Make rs771654971(T;T) |
Reference | GRCh38.p2 38.2/147 |
Chromosome | 17 |
Position | 61683785 |
Gene | BRIP1 |
is a | snp |
is | mentioned by |
dbSNP | rs771654971 |
dbSNP (classic) | rs771654971 |
ClinGen | rs771654971 |
ebi | rs771654971 |
HLI | rs771654971 |
Exac | rs771654971 |
Gnomad | rs771654971 |
Varsome | rs771654971 |
LitVar | rs771654971 |
Map | rs771654971 |
PheGenI | rs771654971 |
Biobank | rs771654971 |
1000 genomes | rs771654971 |
hgdp | rs771654971 |
ensembl | rs771654971 |
geneview | rs771654971 |
scholar | rs771654971 |
rs771654971 | |
pharmgkb | rs771654971 |
gwascentral | rs771654971 |
openSNP | rs771654971 |
23andMe | rs771654971 |
SNPshot | rs771654971 |
SNPdbe | rs771654971 |
MSV3d | rs771654971 |
GWAS Ctlg | rs771654971 |
Max Magnitude | 6 |
ClinVar | |
---|---|
Risk | rs771654971(T;T) |
Alt | rs771654971(T;T) |
Reference | Rs771654971(-;-) |
Significance | Probable-Pathogenic |
Disease | Hereditary cancer-predisposing syndrome |
Variation | info |
Gene | BRIP1 |
CLNDBN | Hereditary cancer-predisposing syndrome |
Reversed | 0 |
HGVS | NC_000017.10:g.59761147dupT |
CLNSRC | |
CLNACC | RCV000219598.1, |