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rs398122729

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs398122729(C;T)
Make rs398122729(T;T)
ReferenceGRCh38 38.1/141
Chromosome13
Position32333120
GeneBRCA2
is asnp
is mentioned by
dbSNPrs398122729
ebirs398122729
HLIrs398122729
Exacrs398122729
Varsomers398122729
Maprs398122729
PheGenIrs398122729
hapmaprs398122729
1000 genomesrs398122729
hgdprs398122729
ensemblrs398122729
gopubmedrs398122729
geneviewrs398122729
scholarrs398122729
googlers398122729
pharmgkbrs398122729
gwascentralrs398122729
openSNPrs398122729
23andMers398122729
23andMe allrs398122729
SNP Nexus

SNPshotrs398122729
SNPdbers398122729
MSV3drs398122729
GWAS Ctlgrs398122729
Max Magnitude0
ClinVar
Risk rs398122729(T;T)
Alt rs398122729(T;T)
Reference rs398122729(C;C)
Significance Pathogenic
Disease Breast-ovarian cancer Hereditary cancer-predisposing syndrome
Variation info
Gene BRCA2
CLNDBN Breast-ovarian cancer, familial 2 Hereditary cancer-predisposing syndrome
Reversed 0
HGVS NC_000013.10:g.32907257C>T
CLNSRC Ambry Genetics ClinVar
CLNACC RCV000077662.2, RCV000130404.2,