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rs398124075

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(CT;CT) 0 common in clinvar
Make rs398124075(-;-)
Make rs398124075(-;CT)
ReferenceGRCh38 38.1/141
ChromosomeX
Position31478998
GeneDMD
is asnp
is mentioned by
dbSNPrs398124075
ebirs398124075
HLIrs398124075
Exacrs398124075
Varsomers398124075
Maprs398124075
PheGenIrs398124075
hapmaprs398124075
1000 genomesrs398124075
hgdprs398124075
ensemblrs398124075
gopubmedrs398124075
geneviewrs398124075
scholarrs398124075
googlers398124075
pharmgkbrs398124075
gwascentralrs398124075
openSNPrs398124075
23andMers398124075
23andMe allrs398124075
SNP Nexus

SNPshotrs398124075
SNPdbers398124075
MSV3drs398124075
GWAS Ctlgrs398124075
Max Magnitude0
ClinVar
Risk rs398124075(;)
Alt rs398124075(;)
Reference rs398124075(CT;CT)
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.31497115_31497116delAG
CLNSRC ClinVar
CLNACC RCV000080804.4, RCV000179205.1, RCV000179206.1,