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rs398124092

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs398124092(C;T)
Make rs398124092(T;T)
ReferenceGRCh38 38.1/141
ChromosomeX
Position31223071
GeneDMD
is asnp
is mentioned by
dbSNPrs398124092
ebirs398124092
HLIrs398124092
Exacrs398124092
Varsomers398124092
Maprs398124092
PheGenIrs398124092
hapmaprs398124092
1000 genomesrs398124092
hgdprs398124092
ensemblrs398124092
gopubmedrs398124092
geneviewrs398124092
scholarrs398124092
googlers398124092
pharmgkbrs398124092
gwascentralrs398124092
openSNPrs398124092
23andMers398124092
23andMe allrs398124092
SNP Nexus

SNPshotrs398124092
SNPdbers398124092
MSV3drs398124092
GWAS Ctlgrs398124092
Max Magnitude0
ClinVar
Risk rs398124092(T;T)
Alt rs398124092(T;T)
Reference rs398124092(C;C)
Significance Pathogenic
Disease Dilated cardiomyopathy 3B Becker muscular dystrophy Duchenne muscular dystrophy
Variation info
Gene DMD
CLNDBN Dilated cardiomyopathy 3B Becker muscular dystrophy Duchenne muscular dystrophy
Reversed 1
HGVS NC_000023.10:g.31241188G>A
CLNSRC HGMD
CLNACC RCV000080837.4, RCV000179640.1, RCV000179641.2,