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rs80359083

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs80359083(A;A)
Make rs80359083(A;G)
ReferenceGRCh38 38.1/141
Chromosome13
Position32370448
GeneBRCA2
is asnp
is mentioned by
dbSNPrs80359083
ebirs80359083
HLIrs80359083
Exacrs80359083
Varsomers80359083
Maprs80359083
PheGenIrs80359083
hapmaprs80359083
1000 genomesrs80359083
hgdprs80359083
ensemblrs80359083
gopubmedrs80359083
geneviewrs80359083
scholarrs80359083
googlers80359083
pharmgkbrs80359083
gwascentralrs80359083
openSNPrs80359083
23andMers80359083
23andMe allrs80359083
SNP Nexus

SNPshotrs80359083
SNPdbers80359083
MSV3drs80359083
GWAS Ctlgrs80359083
Max Magnitude0
ClinVar
Risk rs80359083(A,T;A,T)
Alt rs80359083(A,T;A,T)
Reference rs80359083(G;G)
Significance Untested
Disease Breast-ovarian cancer Hereditary breast and ovarian cancer syndrome Hereditary cancer-predisposing syndrome
Variation info
Gene BRCA2
CLNDBN Breast-ovarian cancer, familial 2 Hereditary breast and ovarian cancer syndrome Hereditary cancer-predisposing syndrome
Reversed 0
HGVS NC_000013.10:g.32944585G>A; NC_000013.10:g.32944585G>T
CLNSRC ClinVar
CLNACC RCV000031740.5, RCV000045500.3, RCV000165807.1, RCV000031741.3,