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rs80358766

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs80358766(A;A)
Make rs80358766(A;G)
ReferenceGRCh38 38.1/141
Chromosome13
Position32339783
GeneBRCA2
is asnp
is mentioned by
dbSNPrs80358766
ebirs80358766
HLIrs80358766
Exacrs80358766
Varsomers80358766
Maprs80358766
PheGenIrs80358766
hapmaprs80358766
1000 genomesrs80358766
hgdprs80358766
ensemblrs80358766
gopubmedrs80358766
geneviewrs80358766
scholarrs80358766
googlers80358766
pharmgkbrs80358766
gwascentralrs80358766
openSNPrs80358766
23andMers80358766
23andMe allrs80358766
SNP Nexus

SNPshotrs80358766
SNPdbers80358766
MSV3drs80358766
GWAS Ctlgrs80358766
Max Magnitude0
ClinVar
Risk rs80358766(A;A)
Alt rs80358766(A;A)
Reference rs80358766(G;G)
Significance Other
Disease Hereditary breast and ovarian cancer syndrome Breast-ovarian cancer Tumor susceptibility linked to germline BAP1 mutations not specified
Variation info
Gene BRCA2
CLNDBN Hereditary breast and ovarian cancer syndrome Breast-ovarian cancer, familial 2 Tumor susceptibility linked to germline BAP1 mutations not specified
Reversed 0
HGVS NC_000013.10:g.32913920G>A
CLNSRC ClinVar
CLNACC RCV000044658.3, RCV000077352.6, RCV000214539.1, RCV000219100.1,