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rs398124050

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs398124050(C;T)
Make rs398124050(T;T)
ReferenceGRCh38 38.1/141
ChromosomeX
Position31729634
GeneDMD
is asnp
is mentioned by
dbSNPrs398124050
ebirs398124050
HLIrs398124050
Exacrs398124050
Varsomers398124050
Maprs398124050
PheGenIrs398124050
hapmaprs398124050
1000 genomesrs398124050
hgdprs398124050
ensemblrs398124050
gopubmedrs398124050
geneviewrs398124050
scholarrs398124050
googlers398124050
pharmgkbrs398124050
gwascentralrs398124050
openSNPrs398124050
23andMers398124050
23andMe allrs398124050
SNP Nexus

SNPshotrs398124050
SNPdbers398124050
MSV3drs398124050
GWAS Ctlgrs398124050
Max Magnitude0
ClinVar
Risk rs398124050(T;T)
Alt rs398124050(T;T)
Reference rs398124050(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.31747751G>A
CLNSRC HGMD
CLNACC RCV000080765.4, RCV000179106.1, RCV000179107.1,