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rs398124038

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs398124038(G;T)
Make rs398124038(T;T)
ReferenceGRCh38 38.1/141
ChromosomeX
Position31875343
GeneDMD
is asnp
is mentioned by
dbSNPrs398124038
ebirs398124038
HLIrs398124038
Exacrs398124038
Varsomers398124038
Maprs398124038
PheGenIrs398124038
hapmaprs398124038
1000 genomesrs398124038
hgdprs398124038
ensemblrs398124038
gopubmedrs398124038
geneviewrs398124038
scholarrs398124038
googlers398124038
pharmgkbrs398124038
gwascentralrs398124038
openSNPrs398124038
23andMers398124038
23andMe allrs398124038
SNP Nexus

SNPshotrs398124038
SNPdbers398124038
MSV3drs398124038
GWAS Ctlgrs398124038
Max Magnitude0
ClinVar
Risk rs398124038(T;T)
Alt rs398124038(T;T)
Reference rs398124038(G;G)
Significance Pathogenic
Disease Dilated cardiomyopathy 3B
Variation info
Gene DMD
CLNDBN Dilated cardiomyopathy 3B
Reversed 1
HGVS NC_000023.10:g.31893460C>A
CLNSRC HGMD
CLNACC RCV000080745.3,