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rs80359039

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs80359039(A;G)
Make rs80359039(G;G)
ReferenceGRCh38 38.1/141
Chromosome13
Position32363234
GeneBRCA2
is asnp
is mentioned by
dbSNPrs80359039
dbSNP (classic)rs80359039
ClinGenrs80359039
ebirs80359039
HLIrs80359039
Exacrs80359039
Gnomadrs80359039
Varsomers80359039
LitVarrs80359039
Maprs80359039
PheGenIrs80359039
Biobankrs80359039
1000 genomesrs80359039
hgdprs80359039
ensemblrs80359039
geneviewrs80359039
scholarrs80359039
googlers80359039
pharmgkbrs80359039
gwascentralrs80359039
openSNPrs80359039
23andMers80359039
SNPshotrs80359039
SNPdbers80359039
MSV3drs80359039
GWAS Ctlgrs80359039
Max Magnitude0
ClinVar
Risk rs80359039(G;G)
Alt rs80359039(G;G)
Reference Rs80359039(A;A)
Significance Untested
Disease Hereditary breast and ovarian cancer syndrome Breast-ovarian cancer
Variation info
Gene BRCA2
CLNDBN Hereditary breast and ovarian cancer syndrome Breast-ovarian cancer, familial 2
Reversed 0
HGVS NC_000013.10:g.32937371A>G
CLNSRC ClinVar
CLNACC RCV000045394.3, RCV000077424.3,