rs878853561
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(G;G) | 0 | common in clinvar |
(G;T) | 6 | BRCA2 variant considered pathogenic for breast cancer |
Make rs878853561(T;T) |
Reference | GRCh38.p2 38.2/147 |
Chromosome | 13 |
Position | 32336594 |
Gene | BRCA2 |
is a | snp |
is | mentioned by |
dbSNP | rs878853561 |
dbSNP (classic) | rs878853561 |
ClinGen | rs878853561 |
ebi | rs878853561 |
HLI | rs878853561 |
Exac | rs878853561 |
Gnomad | rs878853561 |
Varsome | rs878853561 |
LitVar | rs878853561 |
Map | rs878853561 |
PheGenI | rs878853561 |
Biobank | rs878853561 |
1000 genomes | rs878853561 |
hgdp | rs878853561 |
ensembl | rs878853561 |
geneview | rs878853561 |
scholar | rs878853561 |
rs878853561 | |
pharmgkb | rs878853561 |
gwascentral | rs878853561 |
openSNP | rs878853561 |
23andMe | rs878853561 |
SNPshot | rs878853561 |
SNPdbe | rs878853561 |
MSV3d | rs878853561 |
GWAS Ctlg | rs878853561 |
Max Magnitude | 6 |
ClinVar | |
---|---|
Risk | rs878853561(A;A) rs878853561(T;T) |
Alt | rs878853561(A;A) rs878853561(T;T) |
Reference | Rs878853561(G;G) |
Significance | Pathogenic |
Disease | not specified Hereditary breast and ovarian cancer syndrome |
Variation | info |
Gene | BRCA2 |
CLNDBN | not specified Hereditary breast and ovarian cancer syndrome |
Reversed | 0 |
HGVS | NC_000013.10:g.32910731G>A; NC_000013.10:g.32910731G>T |
CLNSRC | |
CLNACC | RCV000431436.1, RCV000229810.1, |