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rs398124004

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs398124004(A;A)
Make rs398124004(A;T)
ReferenceGRCh38 38.1/141
ChromosomeX
Position32809527
GeneDMD
is asnp
is mentioned by
dbSNPrs398124004
ebirs398124004
HLIrs398124004
Exacrs398124004
Varsomers398124004
Maprs398124004
PheGenIrs398124004
hapmaprs398124004
1000 genomesrs398124004
hgdprs398124004
ensemblrs398124004
gopubmedrs398124004
geneviewrs398124004
scholarrs398124004
googlers398124004
pharmgkbrs398124004
gwascentralrs398124004
openSNPrs398124004
23andMers398124004
23andMe allrs398124004
SNP Nexus

SNPshotrs398124004
SNPdbers398124004
MSV3drs398124004
GWAS Ctlgrs398124004
Max Magnitude0
ClinVar
Risk rs398124004(A;A)
Alt rs398124004(A;A)
Reference rs398124004(T;T)
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.32827644A>T
CLNSRC HGMD
CLNACC RCV000080684.4, RCV000179872.1, RCV000179873.1,