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rs398124070

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(AA;AA) 0 common in clinvar
Make rs398124070(-;-)
Make rs398124070(-;AA)
ReferenceGRCh38 38.1/141
ChromosomeX
Position31507296
GeneDMD
is asnp
is mentioned by
dbSNPrs398124070
ebirs398124070
HLIrs398124070
Exacrs398124070
Varsomers398124070
Maprs398124070
PheGenIrs398124070
hapmaprs398124070
1000 genomesrs398124070
hgdprs398124070
ensemblrs398124070
gopubmedrs398124070
geneviewrs398124070
scholarrs398124070
googlers398124070
pharmgkbrs398124070
gwascentralrs398124070
openSNPrs398124070
23andMers398124070
23andMe allrs398124070
SNP Nexus

SNPshotrs398124070
SNPdbers398124070
MSV3drs398124070
GWAS Ctlgrs398124070
Max Magnitude0
ClinVar
Risk rs398124070(;)
Alt rs398124070(;)
Reference rs398124070(AA;AA)
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.31525413_31525414delTT
CLNSRC ClinVar
CLNACC RCV000080797.4, RCV000179177.1, RCV000179178.1,