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rs80359808

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs80359808(A;A)
Make rs80359808(A;G)
ReferenceGRCh38 38.1/142
Chromosome13
Position32394933
GeneBRCA2
is asnp
is mentioned by
dbSNPrs80359808
ebirs80359808
HLIrs80359808
Exacrs80359808
Varsomers80359808
Maprs80359808
PheGenIrs80359808
hapmaprs80359808
1000 genomesrs80359808
hgdprs80359808
ensemblrs80359808
gopubmedrs80359808
geneviewrs80359808
scholarrs80359808
googlers80359808
pharmgkbrs80359808
gwascentralrs80359808
openSNPrs80359808
23andMers80359808
23andMe allrs80359808
SNP Nexus

SNPshotrs80359808
SNPdbers80359808
MSV3drs80359808
GWAS Ctlgrs80359808
Max Magnitude0
ClinVar
Risk rs80359808(A;A)
Alt rs80359808(A;A)
Reference rs80359808(G;G)
Significance Pathogenic
Disease Familial cancer of breast Breast-ovarian cancer not specified
Variation info
Gene BRCA2
CLNDBN Familial cancer of breast Breast-ovarian cancer, familial 2 not specified
Reversed 0
HGVS NC_000013.10:g.32969070G>A; NC_000013.10:g.32969070G>C
CLNSRC ClinVar
CLNACC RCV000045841.2, RCV000114122.1, RCV000216268.1, RCV000238800.1,