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rs398124054

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(;) 0 common in clinvar
Make rs398124054(-;-)
Make rs398124054(-;T)
Make rs398124054(T;T)
ReferenceGRCh38 38.1/141
ChromosomeX
Position31679482
GeneDMD
is asnp
is mentioned by
dbSNPrs398124054
ebirs398124054
HLIrs398124054
Exacrs398124054
Varsomers398124054
Maprs398124054
PheGenIrs398124054
hapmaprs398124054
1000 genomesrs398124054
hgdprs398124054
ensemblrs398124054
gopubmedrs398124054
geneviewrs398124054
scholarrs398124054
googlers398124054
pharmgkbrs398124054
gwascentralrs398124054
openSNPrs398124054
23andMers398124054
23andMe allrs398124054
SNP Nexus

SNPshotrs398124054
SNPdbers398124054
MSV3drs398124054
GWAS Ctlgrs398124054
Max Magnitude0
ClinVar
Risk rs398124054(T;T)
Alt rs398124054(T;T)
Reference Rs398124054(;)
Significance Pathogenic
Disease Dilated cardiomyopathy 3B
Variation info
Gene DMD
CLNDBN Dilated cardiomyopathy 3B
Reversed 1
HGVS NC_000023.10:g.31697600dupA
CLNSRC ClinVar
CLNACC RCV000080770.3,