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rs80359182

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs80359182(C;C)
Make rs80359182(C;T)
ReferenceGRCh38 38.1/141
Chromosome13
Position32319100
GeneBRCA2
is asnp
is mentioned by
dbSNPrs80359182
ebirs80359182
HLIrs80359182
Exacrs80359182
Varsomers80359182
Maprs80359182
PheGenIrs80359182
hapmaprs80359182
1000 genomesrs80359182
hgdprs80359182
ensemblrs80359182
gopubmedrs80359182
geneviewrs80359182
scholarrs80359182
googlers80359182
pharmgkbrs80359182
gwascentralrs80359182
openSNPrs80359182
23andMers80359182
23andMe allrs80359182
SNP Nexus

SNPshotrs80359182
SNPdbers80359182
MSV3drs80359182
GWAS Ctlgrs80359182
Max Magnitude0
ClinVar
Risk rs80359182(C;C)
Alt rs80359182(C;C)
Reference rs80359182(T;T)
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.32893237T>C
CLNSRC ClinVar
CLNACC RCV000045746.2, RCV000113123.1,