rs587782612
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(A;T) | 6 | BRCA2 variant considered pathogenic for breast cancer |
(T;T) | 0 | common in clinvar |
Make rs587782612(A;A) |
Reference | GRCh38.p2 38.2/144 |
Chromosome | 13 |
Position | 32396957 |
Gene | BRCA2 |
is a | snp |
is | mentioned by |
dbSNP | rs587782612 |
dbSNP (classic) | rs587782612 |
ClinGen | rs587782612 |
ebi | rs587782612 |
HLI | rs587782612 |
Exac | rs587782612 |
Gnomad | rs587782612 |
Varsome | rs587782612 |
LitVar | rs587782612 |
Map | rs587782612 |
PheGenI | rs587782612 |
Biobank | rs587782612 |
1000 genomes | rs587782612 |
hgdp | rs587782612 |
ensembl | rs587782612 |
geneview | rs587782612 |
scholar | rs587782612 |
rs587782612 | |
pharmgkb | rs587782612 |
gwascentral | rs587782612 |
openSNP | rs587782612 |
23andMe | rs587782612 |
SNPshot | rs587782612 |
SNPdbe | rs587782612 |
MSV3d | rs587782612 |
GWAS Ctlg | rs587782612 |
Max Magnitude | 6 |
ClinVar | |
---|---|
Risk | rs587782612(A;A) |
Alt | rs587782612(A;A) |
Reference | Rs587782612(T;T) |
Significance | Probable-Pathogenic |
Disease | Hereditary cancer-predisposing syndrome |
Variation | info |
Gene | BRCA2 |
CLNDBN | Hereditary cancer-predisposing syndrome |
Reversed | 0 |
HGVS | NC_000013.10:g.32971094T>A |
CLNSRC | |
CLNACC | RCV000131987.3, |