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rs398122733

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs398122733(-;-)
Make rs398122733(-;T)
ReferenceGRCh38 38.1/141
Chromosome13
Position32319195
GeneBRCA2
is asnp
is mentioned by
dbSNPrs398122733
ebirs398122733
HLIrs398122733
Exacrs398122733
Varsomers398122733
Maprs398122733
PheGenIrs398122733
hapmaprs398122733
1000 genomesrs398122733
hgdprs398122733
ensemblrs398122733
gopubmedrs398122733
geneviewrs398122733
scholarrs398122733
googlers398122733
pharmgkbrs398122733
gwascentralrs398122733
openSNPrs398122733
23andMers398122733
23andMe allrs398122733
SNP Nexus

SNPshotrs398122733
SNPdbers398122733
MSV3drs398122733
GWAS Ctlgrs398122733
Max Magnitude0
ClinVar
Risk rs398122733(;)
Alt rs398122733(;)
Reference rs398122733(T;T)
Significance Pathogenic
Disease Breast-ovarian cancer
Variation info
Gene BRCA2
CLNDBN Breast-ovarian cancer, familial 2
Reversed 0
HGVS NC_000013.10:g.32893332delT
CLNSRC ClinVar
CLNACC RCV000077669.2,