rs15869

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
google	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,