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rs9567552

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common/normal
(G;T) 0 benign variant
(T;T) 0 benign variant
ReferenceGRCh38 38.1/141
Chromosome13
Position32316090
GeneBRCA2
is asnp
is mentioned by
dbSNPrs9567552
ebirs9567552
HLIrs9567552
Exacrs9567552
Varsomers9567552
Maprs9567552
PheGenIrs9567552
hapmaprs9567552
1000 genomesrs9567552
hgdprs9567552
ensemblrs9567552
gopubmedrs9567552
geneviewrs9567552
scholarrs9567552
googlers9567552
pharmgkbrs9567552
gwascentralrs9567552
openSNPrs9567552
23andMers9567552
23andMe allrs9567552
SNP Nexus

SNPshotrs9567552
SNPdbers9567552
MSV3drs9567552
GWAS Ctlgrs9567552
GMAF0.2227
Max Magnitude0
? (G;G) (G;T) (T;T) 28

[PMID 20872766] Association analysis of PALB2 and BRCA2 in bipolar disorder and schizophrenia in a Scandinavian case-control sample

[PMID 17428325OA-icon.png] Common variants in the ATM, BRCA1, BRCA2, CHEK2 and TP53 cancer susceptibility genes are unlikely to increase breast cancer risk.

[PMID 19500380OA-icon.png] LD2SNPing: linkage disequilibrium plotter and RFLP enzyme mining for tag SNPs.


ClinVar
Risk rs9567552(T;T)
Alt rs9567552(T;T)
Reference rs9567552(G;G)
Significance Non-pathogenic
Disease Breast-ovarian cancer
Variation info
Gene BRCA2
CLNDBN Breast-ovarian cancer, familial 2
Reversed 0
HGVS NC_000013.10:g.32890227G>T
CLNSRC
CLNACC RCV000191549.1,