rs15869
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(A;A) | 0 | common in clinvar |
Make rs15869(A;C) |
Make rs15869(C;C) |
Reference | GRCh38.p2 38.2/146 |
Chromosome | 13 |
Position | 32398875 |
Gene | BRCA2 |
is a | snp |
is | mentioned by |
dbSNP | rs15869 |
dbSNP (classic) | rs15869 |
ClinGen | rs15869 |
ebi | rs15869 |
HLI | rs15869 |
Exac | rs15869 |
Gnomad | rs15869 |
Varsome | rs15869 |
LitVar | rs15869 |
Map | rs15869 |
PheGenI | rs15869 |
Biobank | rs15869 |
1000 genomes | rs15869 |
hgdp | rs15869 |
ensembl | rs15869 |
geneview | rs15869 |
scholar | rs15869 |
rs15869 | |
pharmgkb | rs15869 |
gwascentral | rs15869 |
openSNP | rs15869 |
23andMe | rs15869 |
SNPshot | rs15869 |
SNPdbe | rs15869 |
MSV3d | rs15869 |
GWAS Ctlg | rs15869 |
Max Magnitude | 0 |
? | (A;A) (A;C) (C;C) | 28 |
---|---|---|
|
[PMID 26711789] A variant at a potentially functional microRNA-binding site in BRIP1 was associated with risk of squamous cell carcinoma of the head and neck.
ClinVar | |
---|---|
Risk | rs15869(C;C) |
Alt | rs15869(C;C) |
Reference | Rs15869(A;A) |
Significance | Non-pathogenic |
Disease | Breast-ovarian cancer Fanconi anemia Hereditary breast and ovarian cancer syndrome |
Variation | info |
Gene | BRCA2 |
CLNDBN | Breast-ovarian cancer, familial 2 Fanconi anemia Hereditary breast and ovarian cancer syndrome |
Reversed | 0 |
HGVS | NC_000013.10:g.32973012A>C |
CLNSRC | Breast Cancer Information Core (BRCA2) |
CLNACC | RCV000112856.2, RCV000273093.1, RCV000328172.1, |