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rs80359026

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs80359026(A;G)
Make rs80359026(G;G)
ReferenceGRCh38 38.1/141
Chromosome13
Position32362692
GeneBRCA2
is asnp
is mentioned by
dbSNPrs80359026
ebirs80359026
HLIrs80359026
Exacrs80359026
Varsomers80359026
Maprs80359026
PheGenIrs80359026
hapmaprs80359026
1000 genomesrs80359026
hgdprs80359026
ensemblrs80359026
gopubmedrs80359026
geneviewrs80359026
scholarrs80359026
googlers80359026
pharmgkbrs80359026
gwascentralrs80359026
openSNPrs80359026
23andMers80359026
23andMe allrs80359026
SNP Nexus

SNPshotrs80359026
SNPdbers80359026
MSV3drs80359026
GWAS Ctlgrs80359026
Max Magnitude0
ClinVar
Risk rs80359026(G;G)
Alt rs80359026(G;G)
Reference rs80359026(A;A)
Significance Untested
Disease Breast-ovarian cancer Familial cancer of breast
Variation info
Gene BRCA2
CLNDBN Breast-ovarian cancer, familial 2 Familial cancer of breast
Reversed 0
HGVS NC_000013.10:g.32936829A>G
CLNSRC ClinVar
CLNACC RCV000031712.4, RCV000045361.2,