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rs80359063

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs80359063(G;T)
Make rs80359063(T;T)
ReferenceGRCh38 38.1/141
Chromosome13
Position32363373
GeneBRCA2
is asnp
is mentioned by
dbSNPrs80359063
ClinGenrs80359063
ebirs80359063
HLIrs80359063
Exacrs80359063
Varsomers80359063
Maprs80359063
PheGenIrs80359063
hapmaprs80359063
1000 genomesrs80359063
hgdprs80359063
ensemblrs80359063
gopubmedrs80359063
geneviewrs80359063
scholarrs80359063
googlers80359063
pharmgkbrs80359063
gwascentralrs80359063
openSNPrs80359063
23andMers80359063
23andMe allrs80359063
SNP Nexus

SNPshotrs80359063
SNPdbers80359063
MSV3drs80359063
GWAS Ctlgrs80359063
Max Magnitude0
ClinVar
Risk rs80359063(T;T)
Alt rs80359063(T;T)
Reference Rs80359063(G;G)
Significance Untested
Disease Familial cancer of breast Breast-ovarian cancer
Variation info
Gene BRCA2
CLNDBN Familial cancer of breast Breast-ovarian cancer, familial 2
Reversed 0
HGVS NC_000013.10:g.32937510G>T
CLNSRC ClinVar
CLNACC RCV000045439.2, RCV000113881.1,