rs786201727
From SNPedia
Merged into | rs80359548 |
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(-;-) | 0 | common in clinvar |
(-;T) | 6 | BRCA2 variant considered pathogenic for breast cancer |
Make rs786201727(T;T) |
Reference | GRCh38.p2 38.2/146 |
Chromosome | 13 |
Position | 32340289 |
Gene | BRCA2 |
is a | snp |
is | mentioned by |
dbSNP | rs786201727 |
dbSNP (classic) | rs786201727 |
ClinGen | rs786201727 |
ebi | rs786201727 |
HLI | rs786201727 |
Exac | rs786201727 |
Gnomad | rs786201727 |
Varsome | rs786201727 |
LitVar | rs786201727 |
Map | rs786201727 |
PheGenI | rs786201727 |
Biobank | rs786201727 |
1000 genomes | rs786201727 |
hgdp | rs786201727 |
ensembl | rs786201727 |
geneview | rs786201727 |
scholar | rs786201727 |
rs786201727 | |
pharmgkb | rs786201727 |
gwascentral | rs786201727 |
openSNP | rs786201727 |
23andMe | rs786201727 |
SNPshot | rs786201727 |
SNPdbe | rs786201727 |
MSV3d | rs786201727 |
GWAS Ctlg | rs786201727 |
Status | Merged into rs80359548 |
Max Magnitude | 6 |
ClinVar | |
---|---|
Risk | rs786201727(T;T) |
Alt | rs786201727(T;T) |
Reference | Rs786201727(;) |
Significance | Pathogenic |
Disease | Breast-ovarian cancer Hereditary cancer-predisposing syndrome |
Variation | info |
Gene | BRCA2 |
CLNDBN | Breast-ovarian cancer, familial 2 Hereditary cancer-predisposing syndrome |
Reversed | 0 |
HGVS | NC_000013.10:g.32914426dupT |
CLNSRC | Breast Cancer Information Core (BRCA2) |
CLNACC | RCV000113505.3, RCV000164167.1, |