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rs398124037

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs398124037(-;-)
Make rs398124037(-;A)
ReferenceGRCh38 38.1/141
ChromosomeX
Position31875350
GeneDMD
is asnp
is mentioned by
dbSNPrs398124037
ebirs398124037
HLIrs398124037
Exacrs398124037
Varsomers398124037
Maprs398124037
PheGenIrs398124037
hapmaprs398124037
1000 genomesrs398124037
hgdprs398124037
ensemblrs398124037
gopubmedrs398124037
geneviewrs398124037
scholarrs398124037
googlers398124037
pharmgkbrs398124037
gwascentralrs398124037
openSNPrs398124037
23andMers398124037
23andMe allrs398124037
SNP Nexus

SNPshotrs398124037
SNPdbers398124037
MSV3drs398124037
GWAS Ctlgrs398124037
Max Magnitude0
ClinVar
Risk rs398124037(;)
Alt rs398124037(;)
Reference rs398124037(A;A)
Significance Pathogenic
Disease Dilated cardiomyopathy 3B
Variation info
Gene DMD
CLNDBN Dilated cardiomyopathy 3B
Reversed 1
HGVS NC_000023.10:g.31893467delT
CLNSRC ClinVar
CLNACC RCV000080744.3,