rs886038129
From SNPedia
Merged into | rs276174862 |
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(-;CTCT) | 6 | BRCA2 variant considered pathogenic for breast cancer |
(CTCT;CTCT) | 0 | common in clinvar |
Make rs886038129(-;-) |
Reference | GRCh38.p7 38.3/149 |
Chromosome | 13 |
Position | 32340075 |
Gene | BRCA2 |
is a | snp |
is | mentioned by |
dbSNP | rs886038129 |
dbSNP (classic) | rs886038129 |
ClinGen | rs886038129 |
ebi | rs886038129 |
HLI | rs886038129 |
Exac | rs886038129 |
Gnomad | rs886038129 |
Varsome | rs886038129 |
LitVar | rs886038129 |
Map | rs886038129 |
PheGenI | rs886038129 |
Biobank | rs886038129 |
1000 genomes | rs886038129 |
hgdp | rs886038129 |
ensembl | rs886038129 |
geneview | rs886038129 |
scholar | rs886038129 |
rs886038129 | |
pharmgkb | rs886038129 |
gwascentral | rs886038129 |
openSNP | rs886038129 |
23andMe | rs886038129 |
SNPshot | rs886038129 |
SNPdbe | rs886038129 |
MSV3d | rs886038129 |
GWAS Ctlg | rs886038129 |
Status | Merged into rs276174862 |
Max Magnitude | 6 |
ClinVar | |
---|---|
Risk | |
Alt | |
Reference | Rs886038129(CTCT;CTCT) |
Significance | Pathogenic |
Disease | Familial cancer of breast Breast-ovarian cancer |
Variation | info |
Gene | BRCA2 |
CLNDBN | Familial cancer of breast Breast-ovarian cancer, familial 2 |
Reversed | 0 |
HGVS | NC_000013.10:g.32914212_32914215delCTCT |
CLNSRC | Breast Cancer Information Core (BRCA2) |
CLNACC | RCV000044727.2, RCV000241138.3, |