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rs80359082

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs80359082(A;A)
Make rs80359082(A;G)
ReferenceGRCh38 38.1/141
Chromosome13
Position32370447
GeneBRCA2
is asnp
is mentioned by
dbSNPrs80359082
ebirs80359082
HLIrs80359082
Exacrs80359082
Varsomers80359082
Maprs80359082
PheGenIrs80359082
hapmaprs80359082
1000 genomesrs80359082
hgdprs80359082
ensemblrs80359082
gopubmedrs80359082
geneviewrs80359082
scholarrs80359082
googlers80359082
pharmgkbrs80359082
gwascentralrs80359082
openSNPrs80359082
23andMers80359082
23andMe allrs80359082
SNP Nexus

SNPshotrs80359082
SNPdbers80359082
MSV3drs80359082
GWAS Ctlgrs80359082
Max Magnitude0
ClinVar
Risk rs80359082(A;A)
Alt rs80359082(A;A)
Reference rs80359082(G;G)
Significance Other
Disease Hereditary breast and ovarian cancer syndrome not provided Breast-ovarian cancer Hereditary cancer-predisposing syndrome
Variation info
Gene BRCA2
CLNDBN Hereditary breast and ovarian cancer syndrome not provided Breast-ovarian cancer, familial 2 Hereditary cancer-predisposing syndrome
Reversed 0
HGVS NC_000013.10:g.32944584G>A
CLNSRC Ambry Genetics ClinVar
CLNACC RCV000045499.2, RCV000074556.5, RCV000077437.4, RCV000131353.2,