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rs15869

From SNPedia

Orientationplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs15869(A;C)
Make rs15869(C;C)
ReferenceGRCh38.p2 38.2/146
Chromosome13
Position32398875
GeneBRCA2
is asnp
is mentioned by
dbSNPrs15869
ebirs15869
HLIrs15869
Exacrs15869
Varsomers15869
Maprs15869
PheGenIrs15869
hapmaprs15869
1000 genomesrs15869
hgdprs15869
ensemblrs15869
gopubmedrs15869
geneviewrs15869
scholarrs15869
googlers15869
pharmgkbrs15869
gwascentralrs15869
openSNPrs15869
23andMers15869
23andMe allrs15869
SNP Nexus

SNPshotrs15869
SNPdbers15869
MSV3drs15869
GWAS Ctlgrs15869
Max Magnitude0
? (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
Variation info
Gene BRCA2
CLNDBN Breast-ovarian cancer, familial 2
Reversed 0
HGVS NC_000013.10:g.32973012A>C
CLNSRC Breast Cancer Information Core (BRCA2)
CLNACC RCV000112856.2,