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rs398124060

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(TA;TA) 0 common in clinvar
Make rs398124060(-;-)
Make rs398124060(-;TA)
ReferenceGRCh38 38.1/141
ChromosomeX
Position31627825
GeneDMD
is asnp
is mentioned by
dbSNPrs398124060
ebirs398124060
HLIrs398124060
Exacrs398124060
Varsomers398124060
Maprs398124060
PheGenIrs398124060
hapmaprs398124060
1000 genomesrs398124060
hgdprs398124060
ensemblrs398124060
gopubmedrs398124060
geneviewrs398124060
scholarrs398124060
googlers398124060
pharmgkbrs398124060
gwascentralrs398124060
openSNPrs398124060
23andMers398124060
23andMe allrs398124060
SNP Nexus

SNPshotrs398124060
SNPdbers398124060
MSV3drs398124060
GWAS Ctlgrs398124060
Max Magnitude0
ClinVar
Risk rs398124060(;)
Alt rs398124060(;)
Reference rs398124060(TA;TA)
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.31645942_31645943delTA
CLNSRC HGMD
CLNACC RCV000080778.4, RCV000179165.1, RCV000179166.1,