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rs398123930

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs398123930(A;T)
Make rs398123930(T;T)
ReferenceGRCh38 38.1/141
ChromosomeX
Position33020202
GeneDMD
is asnp
is mentioned by
dbSNPrs398123930
ebirs398123930
HLIrs398123930
Exacrs398123930
Varsomers398123930
Maprs398123930
PheGenIrs398123930
hapmaprs398123930
1000 genomesrs398123930
hgdprs398123930
ensemblrs398123930
gopubmedrs398123930
geneviewrs398123930
scholarrs398123930
googlers398123930
pharmgkbrs398123930
gwascentralrs398123930
openSNPrs398123930
23andMers398123930
23andMe allrs398123930
SNP Nexus

SNPshotrs398123930
SNPdbers398123930
MSV3drs398123930
GWAS Ctlgrs398123930
Max Magnitude0
ClinVar
Risk rs398123930(T;T)
Alt rs398123930(T;T)
Reference rs398123930(A;A)
Significance Pathogenic
Disease Dilated cardiomyopathy 3B
Variation info
Gene DMD
CLNDBN Dilated cardiomyopathy 3B
Reversed 1
HGVS NC_000023.10:g.33038319T>A
CLNSRC ClinVar
CLNACC RCV000080567.3,