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rs80358973

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs80358973(A;A)
Make rs80358973(A;G)
ReferenceGRCh38 38.1/141
Chromosome13
Position32356473
GeneBRCA2
is asnp
is mentioned by
dbSNPrs80358973
ebirs80358973
HLIrs80358973
Exacrs80358973
Varsomers80358973
Maprs80358973
PheGenIrs80358973
hapmaprs80358973
1000 genomesrs80358973
hgdprs80358973
ensemblrs80358973
gopubmedrs80358973
geneviewrs80358973
scholarrs80358973
googlers80358973
pharmgkbrs80358973
gwascentralrs80358973
openSNPrs80358973
23andMers80358973
23andMe allrs80358973
SNP Nexus

SNPshotrs80358973
SNPdbers80358973
MSV3drs80358973
GWAS Ctlgrs80358973
Max Magnitude0
ClinVar
Risk rs80358973(A;A)
Alt rs80358973(A;A)
Reference rs80358973(G;G)
Significance Other
Disease Familial cancer of breast Breast-ovarian cancer Hereditary cancer-predisposing syndrome
Variation info
Gene BRCA2
CLNDBN Familial cancer of breast Breast-ovarian cancer, familial 2 Hereditary cancer-predisposing syndrome
Reversed 0
HGVS NC_000013.10:g.32930610G>A
CLNSRC ClinVar
CLNACC RCV000045228.2, RCV000083135.4, RCV000164832.1,