rs730882169
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 rs730882169(A;A) |
Reference | GRCh38.p2 38.2/144 |
Chromosome | 13 |
Position | 32355119 |
Gene | BRCA2 |
is a | snp |
is | mentioned by |
dbSNP | rs730882169 |
dbSNP (classic) | rs730882169 |
ClinGen | rs730882169 |
ebi | rs730882169 |
HLI | rs730882169 |
Exac | rs730882169 |
Gnomad | rs730882169 |
Varsome | rs730882169 |
LitVar | rs730882169 |
Map | rs730882169 |
PheGenI | rs730882169 |
Biobank | rs730882169 |
1000 genomes | rs730882169 |
hgdp | rs730882169 |
ensembl | rs730882169 |
geneview | rs730882169 |
scholar | rs730882169 |
rs730882169 | |
pharmgkb | rs730882169 |
gwascentral | rs730882169 |
openSNP | rs730882169 |
23andMe | rs730882169 |
SNPshot | rs730882169 |
SNPdbe | rs730882169 |
MSV3d | rs730882169 |
GWAS Ctlg | rs730882169 |
Max Magnitude | 6 |
ClinVar | |
---|---|
Risk | rs730882169(A;A) |
Alt | rs730882169(A;A) |
Reference | Rs730882169(T;T) |
Significance | Pathogenic |
Disease | Breast-ovarian cancer |
Variation | info |
Gene | BRCA2 |
CLNDBN | Breast-ovarian cancer, familial 2 |
Reversed | 0 |
HGVS | NC_000013.10:g.32929256T>A |
CLNSRC | |
CLNACC | RCV000162058.3, |