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rs11571836

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs11571836(A;G)
Make rs11571836(G;G)
ReferenceGRCh38 38.1/141
Chromosome13
Position32399302
GeneBRCA2
is asnp
is mentioned by
dbSNPrs11571836
ebirs11571836
HLIrs11571836
Exacrs11571836
Varsomers11571836
Maprs11571836
PheGenIrs11571836
hapmaprs11571836
1000 genomesrs11571836
hgdprs11571836
ensemblrs11571836
gopubmedrs11571836
geneviewrs11571836
scholarrs11571836
googlers11571836
pharmgkbrs11571836
gwascentralrs11571836
openSNPrs11571836
23andMers11571836
23andMe allrs11571836
SNP Nexus

SNPshotrs11571836
SNPdbers11571836
MSV3drs11571836
GWAS Ctlgrs11571836
GMAF0.2163
Max Magnitude0
? (A;A) (A;G) (G;G) 28
[PMID 22809218OA-icon.png] 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
Variation info
Gene BRCA2
CLNDBN Breast-ovarian cancer, familial 2
Reversed 0
HGVS NC_000013.10:g.32973439A>G
CLNSRC
CLNACC RCV000191876.1,