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rs80359080

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;G) 6 BRCA2 variant considered pathogenic for breast cancer
(G;G) 0 common in clinvar


Make rs80359080(A;A)
ReferenceGRCh38 38.1/141
Chromosome13
Position32370433
GeneBRCA2
is asnp
is mentioned by
dbSNPrs80359080
ebirs80359080
HLIrs80359080
Exacrs80359080
Varsomers80359080
Maprs80359080
PheGenIrs80359080
hapmaprs80359080
1000 genomesrs80359080
hgdprs80359080
ensemblrs80359080
gopubmedrs80359080
geneviewrs80359080
scholarrs80359080
googlers80359080
pharmgkbrs80359080
gwascentralrs80359080
openSNPrs80359080
23andMers80359080
23andMe allrs80359080
SNP Nexus

SNPshotrs80359080
SNPdbers80359080
MSV3drs80359080
GWAS Ctlgrs80359080
Max Magnitude6
ClinVar
Risk rs80359080(A,C,T;A,C,T)
Alt rs80359080(A,C,T;A,C,T)
Reference rs80359080(G;G)
Significance Pathogenic
Disease Familial cancer of breast Breast-ovarian cancer
Variation info
Gene BRCA2
CLNDBN Familial cancer of breast Breast-ovarian cancer, familial 2
Reversed 0
HGVS NC_000013.10:g.32944570G>A; NC_000013.10:g.32944570G>C
CLNSRC ClinVar
CLNACC RCV000045494.2, RCV000162060.1, RCV000045495.2, RCV000113916.1,