rs397507922
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(A;G) | 6 | BRCA2 variant considered pathogenic for breast cancer |
(G;G) | 0 | common in clinvar |
Make rs397507922(A;A) |
Reference | GRCh38 38.1/141 |
Chromosome | 13 |
Position | 32356610 |
Gene | BRCA2 |
is a | snp |
is | mentioned by |
dbSNP | rs397507922 |
dbSNP (classic) | rs397507922 |
ClinGen | rs397507922 |
ebi | rs397507922 |
HLI | rs397507922 |
Exac | rs397507922 |
Gnomad | rs397507922 |
Varsome | rs397507922 |
LitVar | rs397507922 |
Map | rs397507922 |
PheGenI | rs397507922 |
Biobank | rs397507922 |
1000 genomes | rs397507922 |
hgdp | rs397507922 |
ensembl | rs397507922 |
geneview | rs397507922 |
scholar | rs397507922 |
rs397507922 | |
pharmgkb | rs397507922 |
gwascentral | rs397507922 |
openSNP | rs397507922 |
23andMe | rs397507922 |
SNPshot | rs397507922 |
SNPdbe | rs397507922 |
MSV3d | rs397507922 |
GWAS Ctlg | rs397507922 |
Max Magnitude | 6 |
ClinVar | |
---|---|
Risk | rs397507922(A;A) rs397507922(C;C) rs397507922(T;T) |
Alt | rs397507922(A;A) rs397507922(C;C) rs397507922(T;T) |
Reference | Rs397507922(G;G) |
Significance | Pathogenic |
Disease | Hereditary breast and ovarian cancer syndrome Breast-ovarian cancer not provided Familial cancer of breast |
Variation | info |
Gene | BRCA2 |
CLNDBN | Hereditary breast and ovarian cancer syndrome Breast-ovarian cancer, familial 2 not provided Familial cancer of breast |
Reversed | 0 |
HGVS | NC_000013.10:g.32930747G>A; NC_000013.10:g.32930747G>C; NC_000013.10:g.32930747G>T |
CLNSRC | ClinVar |
CLNACC | RCV000045259.3, RCV000083138.4, RCV000486153.1, RCV000235926.1, RCV000045260.2, RCV000258277.1, |