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rs398124078

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(TC;TC) 0 common in clinvar
Make rs398124078(-;-)
Make rs398124078(-;TC)
ReferenceGRCh38 38.1/141
ChromosomeX
Position31478130
GeneDMD
is asnp
is mentioned by
dbSNPrs398124078
ebirs398124078
HLIrs398124078
Exacrs398124078
Varsomers398124078
Maprs398124078
PheGenIrs398124078
hapmaprs398124078
1000 genomesrs398124078
hgdprs398124078
ensemblrs398124078
gopubmedrs398124078
geneviewrs398124078
scholarrs398124078
googlers398124078
pharmgkbrs398124078
gwascentralrs398124078
openSNPrs398124078
23andMers398124078
23andMe allrs398124078
SNP Nexus

SNPshotrs398124078
SNPdbers398124078
MSV3drs398124078
GWAS Ctlgrs398124078
Max Magnitude0
ClinVar
Risk rs398124078(;)
Alt rs398124078(;)
Reference rs398124078(TC;TC)
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.31496247_31496248delGA
CLNSRC HGMD
CLNACC RCV000080816.4, RCV000179222.1, RCV000179223.1,