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rs80359077

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs80359077(C;C)
Make rs80359077(C;G)
ReferenceGRCh38 38.1/141
Chromosome13
Position32370426
GeneBRCA2
is asnp
is mentioned by
dbSNPrs80359077
ebirs80359077
HLIrs80359077
Exacrs80359077
Varsomers80359077
Maprs80359077
PheGenIrs80359077
hapmaprs80359077
1000 genomesrs80359077
hgdprs80359077
ensemblrs80359077
gopubmedrs80359077
geneviewrs80359077
scholarrs80359077
googlers80359077
pharmgkbrs80359077
gwascentralrs80359077
openSNPrs80359077
23andMers80359077
23andMe allrs80359077
SNP Nexus

SNPshotrs80359077
SNPdbers80359077
MSV3drs80359077
GWAS Ctlgrs80359077
Max Magnitude0
ClinVar
Risk rs80359077(A,C;A,C)
Alt rs80359077(A,C;A,C)
Reference rs80359077(G;G)
Significance Other
Disease Familial cancer of breast Breast-ovarian cancer Hereditary cancer-predisposing syndrome not specified
Variation info
Gene BRCA2
CLNDBN Familial cancer of breast Breast-ovarian cancer, familial 2 Hereditary cancer-predisposing syndrome not specified
Reversed 0
HGVS NC_000013.10:g.32944563G>A; NC_000013.10:g.32944563G>C
CLNSRC Ambry Genetics ClinVar
CLNACC RCV000045489.2, RCV000077436.4, RCV000130784.2, RCV000220216.1, RCV000045490.2, RCV000113911.1,