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rs398122741

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs398122741(C;T)
Make rs398122741(T;T)
ReferenceGRCh38 38.1/141
Chromosome13
Position32319226
GeneBRCA2
is asnp
is mentioned by
dbSNPrs398122741
ebirs398122741
HLIrs398122741
Exacrs398122741
Varsomers398122741
Maprs398122741
PheGenIrs398122741
hapmaprs398122741
1000 genomesrs398122741
hgdprs398122741
ensemblrs398122741
gopubmedrs398122741
geneviewrs398122741
scholarrs398122741
googlers398122741
pharmgkbrs398122741
gwascentralrs398122741
openSNPrs398122741
23andMers398122741
23andMe allrs398122741
SNP Nexus

SNPshotrs398122741
SNPdbers398122741
MSV3drs398122741
GWAS Ctlgrs398122741
Max Magnitude0
ClinVar
Risk rs398122741(T;T)
Alt rs398122741(T;T)
Reference rs398122741(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.32893363C>T
CLNSRC ClinVar
CLNACC RCV000077678.2,