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rs398122777

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs398122777(-;-)
Make rs398122777(-;C)
ReferenceGRCh38 38.1/141
Chromosome13
Position32338566
GeneBRCA2
is asnp
is mentioned by
dbSNPrs398122777
ebirs398122777
HLIrs398122777
Exacrs398122777
Varsomers398122777
Maprs398122777
PheGenIrs398122777
hapmaprs398122777
1000 genomesrs398122777
hgdprs398122777
ensemblrs398122777
gopubmedrs398122777
geneviewrs398122777
scholarrs398122777
googlers398122777
pharmgkbrs398122777
gwascentralrs398122777
openSNPrs398122777
23andMers398122777
23andMe allrs398122777
SNP Nexus

SNPshotrs398122777
SNPdbers398122777
MSV3drs398122777
GWAS Ctlgrs398122777
Max Magnitude0
ClinVar
Risk rs398122777(;)
Alt rs398122777(;)
Reference rs398122777(C;C)
Significance Pathogenic
Disease Breast-ovarian cancer
Variation info
Gene BRCA2
CLNDBN Breast-ovarian cancer, familial 2
Reversed 0
HGVS NC_000013.10:g.32912703delC
CLNSRC ClinVar
CLNACC RCV000077723.2,