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rs398124072

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs398124072(C;T)
Make rs398124072(T;T)
ReferenceGRCh38 38.1/141
ChromosomeX
Position31496892
GeneDMD
is asnp
is mentioned by
dbSNPrs398124072
ebirs398124072
HLIrs398124072
Exacrs398124072
Varsomers398124072
Maprs398124072
PheGenIrs398124072
hapmaprs398124072
1000 genomesrs398124072
hgdprs398124072
ensemblrs398124072
gopubmedrs398124072
geneviewrs398124072
scholarrs398124072
googlers398124072
pharmgkbrs398124072
gwascentralrs398124072
openSNPrs398124072
23andMers398124072
23andMe allrs398124072
SNP Nexus

SNPshotrs398124072
SNPdbers398124072
MSV3drs398124072
GWAS Ctlgrs398124072
Max Magnitude0
ClinVar
Risk rs398124072(T;T)
Alt rs398124072(T;T)
Reference rs398124072(C;C)
Significance Pathogenic
Disease Dilated cardiomyopathy 3B Duchenne muscular dystrophy
Variation info
Gene DMD
CLNDBN Dilated cardiomyopathy 3B Duchenne muscular dystrophy
Reversed 1
HGVS NC_000023.10:g.31515009G>A
CLNSRC HGMD
CLNACC RCV000080800.3, RCV000201168.1,