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rs398124005

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs398124005(-;-)
Make rs398124005(-;C)
ReferenceGRCh38 38.1/141
ChromosomeX
Position32287637
GeneDMD
is asnp
is mentioned by
dbSNPrs398124005
ebirs398124005
HLIrs398124005
Exacrs398124005
Varsomers398124005
Maprs398124005
PheGenIrs398124005
hapmaprs398124005
1000 genomesrs398124005
hgdprs398124005
ensemblrs398124005
gopubmedrs398124005
geneviewrs398124005
scholarrs398124005
googlers398124005
pharmgkbrs398124005
gwascentralrs398124005
openSNPrs398124005
23andMers398124005
23andMe allrs398124005
SNP Nexus

SNPshotrs398124005
SNPdbers398124005
MSV3drs398124005
GWAS Ctlgrs398124005
Max Magnitude0
ClinVar
Risk rs398124005(;)
Alt rs398124005(;)
Reference rs398124005(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.32305754delG
CLNSRC HGMD
CLNACC RCV000080685.4, RCV000178526.1, RCV000178527.1,