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rs398122747

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs398122747(-;-)
Make rs398122747(-;A)
ReferenceGRCh38 38.1/141
Chromosome13
Position32336725
GeneBRCA2
is asnp
is mentioned by
dbSNPrs398122747
ebirs398122747
HLIrs398122747
Exacrs398122747
Varsomers398122747
Maprs398122747
PheGenIrs398122747
hapmaprs398122747
1000 genomesrs398122747
hgdprs398122747
ensemblrs398122747
gopubmedrs398122747
geneviewrs398122747
scholarrs398122747
googlers398122747
pharmgkbrs398122747
gwascentralrs398122747
openSNPrs398122747
23andMers398122747
23andMe allrs398122747
SNP Nexus

SNPshotrs398122747
SNPdbers398122747
MSV3drs398122747
GWAS Ctlgrs398122747
Max Magnitude0
ClinVar
Risk rs398122747(;)
Alt rs398122747(;)
Reference rs398122747(A;A)
Significance Pathogenic
Disease Breast-ovarian cancer
Variation info
Gene BRCA2
CLNDBN Breast-ovarian cancer, familial 2
Reversed 0
HGVS NC_000013.10:g.32910862delA
CLNSRC ClinVar
CLNACC RCV000077685.2,