rs886040671
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(-;CC) | 6 | BRCA2 variant considered pathogenic for breast cancer |
(CC;CC) | 0 | common in clinvar |
Make rs886040671(-;-) |
Reference | GRCh38.p7 38.3/149 |
Chromosome | 13 |
Position | 32329475 |
Gene | BRCA2 |
is a | snp |
is | mentioned by |
dbSNP | rs886040671 |
dbSNP (classic) | rs886040671 |
ClinGen | rs886040671 |
ebi | rs886040671 |
HLI | rs886040671 |
Exac | rs886040671 |
Gnomad | rs886040671 |
Varsome | rs886040671 |
LitVar | rs886040671 |
Map | rs886040671 |
PheGenI | rs886040671 |
Biobank | rs886040671 |
1000 genomes | rs886040671 |
hgdp | rs886040671 |
ensembl | rs886040671 |
geneview | rs886040671 |
scholar | rs886040671 |
rs886040671 | |
pharmgkb | rs886040671 |
gwascentral | rs886040671 |
openSNP | rs886040671 |
23andMe | rs886040671 |
SNPshot | rs886040671 |
SNPdbe | rs886040671 |
MSV3d | rs886040671 |
GWAS Ctlg | rs886040671 |
Max Magnitude | 6 |
ClinVar | |
---|---|
Risk | rs886040671(-;-) |
Alt | rs886040671(-;-) |
Reference | Rs886040671(CC;CC) |
Significance | Pathogenic |
Disease | Breast-ovarian cancer |
Variation | info |
Gene | BRCA2 |
CLNDBN | Breast-ovarian cancer, familial 2 |
Reversed | 0 |
HGVS | NC_000013.10:g.32903612_32903613delCC |
CLNSRC | |
CLNACC | RCV000256576.1, |