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rs80359045

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs80359045(C;C)
Make rs80359045(C;T)
ReferenceGRCh38 38.1/141
Chromosome13
Position32363265
GeneBRCA2
is asnp
is mentioned by
dbSNPrs80359045
ebirs80359045
HLIrs80359045
Exacrs80359045
Varsomers80359045
Maprs80359045
PheGenIrs80359045
hapmaprs80359045
1000 genomesrs80359045
hgdprs80359045
ensemblrs80359045
gopubmedrs80359045
geneviewrs80359045
scholarrs80359045
googlers80359045
pharmgkbrs80359045
gwascentralrs80359045
openSNPrs80359045
23andMers80359045
23andMe allrs80359045
SNP Nexus

SNPshotrs80359045
SNPdbers80359045
MSV3drs80359045
GWAS Ctlgrs80359045
Max Magnitude0
ClinVar
Risk rs80359045(C;C)
Alt rs80359045(C;C)
Reference rs80359045(T;T)
Significance Other
Disease Breast-ovarian cancer Familial cancer of breast Tumor susceptibility linked to germline BAP1 mutations
Variation info
Gene BRCA2
CLNDBN Breast-ovarian cancer, familial 2 Familial cancer of breast Tumor susceptibility linked to germline BAP1 mutations
Reversed 0
HGVS NC_000013.10:g.32937402T>C
CLNSRC ClinVar
CLNACC RCV000031719.4, RCV000045408.2, RCV000219486.1,