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rs398124096

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs398124096(A;A)
Make rs398124096(A;G)
ReferenceGRCh38 38.1/141
ChromosomeX
Position31206668
GeneDMD
is asnp
is mentioned by
dbSNPrs398124096
ebirs398124096
HLIrs398124096
Exacrs398124096
Varsomers398124096
Maprs398124096
PheGenIrs398124096
hapmaprs398124096
1000 genomesrs398124096
hgdprs398124096
ensemblrs398124096
gopubmedrs398124096
geneviewrs398124096
scholarrs398124096
googlers398124096
pharmgkbrs398124096
gwascentralrs398124096
openSNPrs398124096
23andMers398124096
23andMe allrs398124096
SNP Nexus

SNPshotrs398124096
SNPdbers398124096
MSV3drs398124096
GWAS Ctlgrs398124096
Max Magnitude0
ClinVar
Risk rs398124096(A;A)
Alt rs398124096(A;A)
Reference rs398124096(G;G)
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.31224785C>T
CLNSRC ClinVar
CLNACC RCV000080843.4, RCV000179662.1, RCV000179663.1,