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rs398122742

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs398122742(A;A)
Make rs398122742(A;T)
ReferenceGRCh38 38.1/141
Chromosome13
Position32336569
GeneBRCA2
is asnp
is mentioned by
dbSNPrs398122742
ebirs398122742
HLIrs398122742
Exacrs398122742
Varsomers398122742
Maprs398122742
PheGenIrs398122742
hapmaprs398122742
1000 genomesrs398122742
hgdprs398122742
ensemblrs398122742
gopubmedrs398122742
geneviewrs398122742
scholarrs398122742
googlers398122742
pharmgkbrs398122742
gwascentralrs398122742
openSNPrs398122742
23andMers398122742
23andMe allrs398122742
SNP Nexus

SNPshotrs398122742
SNPdbers398122742
MSV3drs398122742
GWAS Ctlgrs398122742
Max Magnitude0
ClinVar
Risk rs398122742(A;A)
Alt rs398122742(A;A)
Reference rs398122742(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.32910706T>A
CLNSRC ClinVar
CLNACC RCV000077679.3,