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rs398124059

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs398124059(-;-)
Make rs398124059(-;A)
ReferenceGRCh38 38.1/141
ChromosomeX
Position31658095
GeneDMD
is asnp
is mentioned by
dbSNPrs398124059
ebirs398124059
HLIrs398124059
Exacrs398124059
Varsomers398124059
Maprs398124059
PheGenIrs398124059
hapmaprs398124059
1000 genomesrs398124059
hgdprs398124059
ensemblrs398124059
gopubmedrs398124059
geneviewrs398124059
scholarrs398124059
googlers398124059
pharmgkbrs398124059
gwascentralrs398124059
openSNPrs398124059
23andMers398124059
23andMe allrs398124059
SNP Nexus

SNPshotrs398124059
SNPdbers398124059
MSV3drs398124059
GWAS Ctlgrs398124059
Max Magnitude0
ClinVar
Risk rs398124059(;)
Alt rs398124059(;)
Reference rs398124059(A;A)
Significance Pathogenic
Disease Dilated cardiomyopathy 3B
Variation info
Gene DMD
CLNDBN Dilated cardiomyopathy 3B
Reversed 1
HGVS NC_000023.10:g.31676212delT
CLNSRC ClinVar
CLNACC RCV000080775.3,