rs397508025
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(A;C) | 6 | BRCA2 variant considered pathogenic for breast cancer |
(C;C) | 0 | common in clinvar |
(C;G) | 6 | BRCA2 variant considered pathogenic for breast cancer |
Make rs397508025(A;A) |
Reference | GRCh38 38.1/141 |
Chromosome | 13 |
Position | 32379774 |
Gene | BRCA2 |
is a | snp |
is | mentioned by |
dbSNP | rs397508025 |
dbSNP (classic) | rs397508025 |
ClinGen | rs397508025 |
ebi | rs397508025 |
HLI | rs397508025 |
Exac | rs397508025 |
Gnomad | rs397508025 |
Varsome | rs397508025 |
LitVar | rs397508025 |
Map | rs397508025 |
PheGenI | rs397508025 |
Biobank | rs397508025 |
1000 genomes | rs397508025 |
hgdp | rs397508025 |
ensembl | rs397508025 |
geneview | rs397508025 |
scholar | rs397508025 |
rs397508025 | |
pharmgkb | rs397508025 |
gwascentral | rs397508025 |
openSNP | rs397508025 |
23andMe | rs397508025 |
SNPshot | rs397508025 |
SNPdbe | rs397508025 |
MSV3d | rs397508025 |
GWAS Ctlg | rs397508025 |
Max Magnitude | 6 |
ClinVar | |
---|---|
Risk | rs397508025(A;A) rs397508025(G;G) |
Alt | rs397508025(A;A) rs397508025(G;G) |
Reference | Rs397508025(C;C) |
Significance | Pathogenic |
Disease | Familial cancer of breast Breast-ovarian cancer not provided Hereditary cancer-predisposing syndrome |
Variation | info |
Gene | BRCA2 |
CLNDBN | Familial cancer of breast Breast-ovarian cancer, familial 2 not provided Hereditary cancer-predisposing syndrome |
Reversed | 0 |
HGVS | NC_000013.10:g.32953911C>A; NC_000013.10:g.32953911C>G |
CLNSRC | ClinVar |
CLNACC | RCV000045677.2, RCV000256867.2, RCV000160161.2, RCV000221983.1, RCV000241294.1, |