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rs398122612

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs398122612(-;-)
Make rs398122612(-;C)
ReferenceGRCh38 38.1/141
Chromosome13
Position32394808
GeneBRCA2
is asnp
is mentioned by
dbSNPrs398122612
ebirs398122612
HLIrs398122612
Exacrs398122612
Varsomers398122612
Maprs398122612
PheGenIrs398122612
hapmaprs398122612
1000 genomesrs398122612
hgdprs398122612
ensemblrs398122612
gopubmedrs398122612
geneviewrs398122612
scholarrs398122612
googlers398122612
pharmgkbrs398122612
gwascentralrs398122612
openSNPrs398122612
23andMers398122612
23andMe allrs398122612
SNP Nexus

SNPshotrs398122612
SNPdbers398122612
MSV3drs398122612
GWAS Ctlgrs398122612
Max Magnitude0
ClinVar
Risk rs398122612(;)
Alt rs398122612(;)
Reference rs398122612(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.32968945delC
CLNSRC ClinVar
CLNACC RCV000077040.2,