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rs80359009

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs80359009(A;A)
Make rs80359009(A;G)
ReferenceGRCh38 38.1/141
Chromosome13
Position32362543
GeneBRCA2
is asnp
is mentioned by
dbSNPrs80359009
ebirs80359009
HLIrs80359009
Exacrs80359009
Varsomers80359009
Maprs80359009
PheGenIrs80359009
hapmaprs80359009
1000 genomesrs80359009
hgdprs80359009
ensemblrs80359009
gopubmedrs80359009
geneviewrs80359009
scholarrs80359009
googlers80359009
pharmgkbrs80359009
gwascentralrs80359009
openSNPrs80359009
23andMers80359009
23andMe allrs80359009
SNP Nexus

SNPshotrs80359009
SNPdbers80359009
MSV3drs80359009
GWAS Ctlgrs80359009
Max Magnitude0
ClinVar
Risk rs80359009(A,C;A,C)
Alt rs80359009(A,C;A,C)
Reference rs80359009(G;G)
Significance Untested
Disease Familial cancer of breast Breast-ovarian cancer Tumor susceptibility linked to germline BAP1 mutations
Variation info
Gene BRCA2
CLNDBN Familial cancer of breast Breast-ovarian cancer, familial 2 Tumor susceptibility linked to germline BAP1 mutations
Reversed 0
HGVS NC_000013.10:g.32936680G>A; NC_000013.10:g.32936680G>C; NC_000013.10:g.32936680G>T
CLNSRC ClinVar
CLNACC RCV000045326.2, RCV000113831.1, RCV000031702.3, RCV000216317.1,