rs11571836

Orientation

plus

Stabilized

plus

Geno	Mag	Summary
(A;A)	0	common in clinvar

Make rs11571836(A;G)

Make rs11571836(G;G)

Reference

GRCh38 38.1/141

Chromosome

13

Position

32399302

Gene

BRCA2

is a	snp
is	mentioned by
dbSNP	rs11571836
dbSNP (classic)	rs11571836
ClinGen	rs11571836
ebi	rs11571836
HLI	rs11571836
Exac	rs11571836
Gnomad	rs11571836
Varsome	rs11571836
LitVar	rs11571836
Map	rs11571836
PheGenI	rs11571836
Biobank	rs11571836
1000 genomes	rs11571836
hgdp	rs11571836
ensembl	rs11571836
geneview	rs11571836
scholar	rs11571836
google	rs11571836
pharmgkb	rs11571836
gwascentral	rs11571836
openSNP	rs11571836
23andMe	rs11571836
SNPshot	rs11571836
SNPdbe	rs11571836
MSV3d	rs11571836
GWAS Ctlg	rs11571836

GMAF

0.2163

Max Magnitude

0

?	(A;A) (A;G) (G;G)	28

[PMID 22809218] BRCA2 variants and cardiovascular disease in a multi-ethnic study

[PMID 23299404] Identification of common variants in BRCA2 and MAP2K4 for susceptibility to sporadic pancreatic cancer.

ClinVar
Risk	rs11571836(G;G)
Alt	rs11571836(G;G)
Reference	Rs11571836(A;A)
Significance	Non-pathogenic
Disease	Breast-ovarian cancer Hereditary breast and ovarian cancer syndrome Fanconi anemia
Variation	info
Gene	BRCA2
CLNDBN	Breast-ovarian cancer, familial 2 Hereditary breast and ovarian cancer syndrome Fanconi anemia
Reversed	0
HGVS	NC_000013.10:g.32973439A>G
CLNSRC
CLNACC	RCV000191876.1, RCV000279399.1, RCV000341382.1,