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rs398124099

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs398124099(C;T)
Make rs398124099(T;T)
ReferenceGRCh38 38.1/141
ChromosomeX
Position32650983
GeneDMD
is asnp
is mentioned by
dbSNPrs398124099
dbSNP (old)rs398124099
ClinGenrs398124099
ebirs398124099
HLIrs398124099
Exacrs398124099
Gnomadrs398124099
Varsomers398124099
Maprs398124099
PheGenIrs398124099
Biobankrs398124099
1000 genomesrs398124099
hgdprs398124099
ensemblrs398124099
gopubmedrs398124099
geneviewrs398124099
scholarrs398124099
googlers398124099
pharmgkbrs398124099
gwascentralrs398124099
openSNPrs398124099
23andMers398124099
23andMe allrs398124099
SNP Nexus

SNPshotrs398124099
SNPdbers398124099
MSV3drs398124099
GWAS Ctlgrs398124099
Max Magnitude0
ClinVar
Risk rs398124099(T;T)
Alt rs398124099(T;T)
Reference Rs398124099(C;C)
Significance Pathogenic
Disease Dilated cardiomyopathy 3B
Variation info
Gene DMD
CLNDBN Dilated cardiomyopathy 3B
Reversed 1
HGVS NC_000023.10:g.32669100G>A
CLNSRC HGMD
CLNACC RCV000080848.3,