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rs80358702

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs80358702(A;A)
Make rs80358702(A;G)
ReferenceGRCh38 38.1/142
Chromosome13
Position32326150
GeneBRCA2
is asnp
is mentioned by
dbSNPrs80358702
ebirs80358702
HLIrs80358702
Exacrs80358702
Varsomers80358702
Maprs80358702
PheGenIrs80358702
hapmaprs80358702
1000 genomesrs80358702
hgdprs80358702
ensemblrs80358702
gopubmedrs80358702
geneviewrs80358702
scholarrs80358702
googlers80358702
pharmgkbrs80358702
gwascentralrs80358702
openSNPrs80358702
23andMers80358702
23andMe allrs80358702
SNP Nexus

SNPshotrs80358702
SNPdbers80358702
MSV3drs80358702
GWAS Ctlgrs80358702
Max Magnitude0
ClinVar
Risk rs80358702(A;A)
Alt rs80358702(A;A)
Reference rs80358702(G;G)
Significance Pathogenic
Disease Familial cancer of breast Breast-ovarian cancer Tumor susceptibility linked to germline BAP1 mutations not provided
Variation info
Gene BRCA2
CLNDBN Familial cancer of breast Breast-ovarian cancer, familial 2 Tumor susceptibility linked to germline BAP1 mutations not provided
Reversed 0
HGVS NC_000013.10:g.32900287G>A
CLNSRC ClinVar
CLNACC RCV000044486.2, RCV000113649.1, RCV000218417.1, RCV000236273.1,