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rs80359024

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs80359024(A;G)
Make rs80359024(G;G)
ReferenceGRCh38 38.1/141
Chromosome13
Position32362681
GeneBRCA2
is asnp
is mentioned by
dbSNPrs80359024
ebirs80359024
HLIrs80359024
Exacrs80359024
Varsomers80359024
Maprs80359024
PheGenIrs80359024
hapmaprs80359024
1000 genomesrs80359024
hgdprs80359024
ensemblrs80359024
gopubmedrs80359024
geneviewrs80359024
scholarrs80359024
googlers80359024
pharmgkbrs80359024
gwascentralrs80359024
openSNPrs80359024
23andMers80359024
23andMe allrs80359024
SNP Nexus

SNPshotrs80359024
SNPdbers80359024
MSV3drs80359024
GWAS Ctlgrs80359024
Max Magnitude0
ClinVar
Risk rs80359024(G;G)
Alt rs80359024(G;G)
Reference rs80359024(A;A)
Significance Probable-Pathogenic
Disease Familial cancer of breast Breast-ovarian cancer not provided
Variation info
Gene BRCA2
CLNDBN Familial cancer of breast Breast-ovarian cancer, familial 2 not provided
Reversed 0
HGVS NC_000013.10:g.32936818A>G
CLNSRC ClinVar
CLNACC RCV000045359.4, RCV000113846.1, RCV000212265.1,