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rs398124084

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs398124084(A;G)
Make rs398124084(G;G)
ReferenceGRCh38 38.1/141
ChromosomeX
Position31261664
GeneDMD
is asnp
is mentioned by
dbSNPrs398124084
ebirs398124084
HLIrs398124084
Exacrs398124084
Varsomers398124084
Maprs398124084
PheGenIrs398124084
hapmaprs398124084
1000 genomesrs398124084
hgdprs398124084
ensemblrs398124084
gopubmedrs398124084
geneviewrs398124084
scholarrs398124084
googlers398124084
pharmgkbrs398124084
gwascentralrs398124084
openSNPrs398124084
23andMers398124084
23andMe allrs398124084
SNP Nexus

SNPshotrs398124084
SNPdbers398124084
MSV3drs398124084
GWAS Ctlgrs398124084
Max Magnitude0
ClinVar
Risk rs398124084(G;G)
Alt rs398124084(G;G)
Reference rs398124084(A;A)
Significance Pathogenic
Disease Dilated cardiomyopathy 3B
Variation info
Gene DMD
CLNDBN Dilated cardiomyopathy 3B
Reversed 1
HGVS NC_000023.10:g.31279781T>C
CLNSRC HGMD
CLNACC RCV000080825.3,