rs730881612
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(-;-) | 0 | common in clinvar |
(-;G) | 6 | Likely miscall in Ancestry v2c data; otherwise, BRCA2 variant considered pathogenic for breast cancer |
Make rs730881612(G;G) |
Reference | GRCh38.p2 38.2/144 |
Chromosome | 13 |
Position | 32355233 |
Gene | BRCA2 |
is a | snp |
is | mentioned by |
dbSNP | rs730881612 |
dbSNP (classic) | rs730881612 |
ClinGen | rs730881612 |
ebi | rs730881612 |
HLI | rs730881612 |
Exac | rs730881612 |
Gnomad | rs730881612 |
Varsome | rs730881612 |
LitVar | rs730881612 |
Map | rs730881612 |
PheGenI | rs730881612 |
Biobank | rs730881612 |
1000 genomes | rs730881612 |
hgdp | rs730881612 |
ensembl | rs730881612 |
geneview | rs730881612 |
scholar | rs730881612 |
rs730881612 | |
pharmgkb | rs730881612 |
gwascentral | rs730881612 |
openSNP | rs730881612 |
23andMe | rs730881612 |
SNPshot | rs730881612 |
SNPdbe | rs730881612 |
MSV3d | rs730881612 |
GWAS Ctlg | rs730881612 |
Max Magnitude | 6 |
aka c.7380_7381insG
ClinVar | |
---|---|
Risk | rs730881612(G;G) |
Alt | rs730881612(G;G) |
Reference | Rs730881612(-;-) |
Significance | Pathogenic |
Disease | Familial cancer of breast |
Variation | info |
Gene | BRCA2 |
CLNDBN | Familial cancer of breast |
Reversed | 0 |
HGVS | NC_000013.10:g.32929370_32929371insG |
CLNSRC | |
CLNACC | RCV000160304.1, |