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rs398124057

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs398124057(-;-)
Make rs398124057(-;G)
ReferenceGRCh38 38.1/141
ChromosomeX
Position31679393
GeneDMD
is asnp
is mentioned by
dbSNPrs398124057
ebirs398124057
HLIrs398124057
Exacrs398124057
Varsomers398124057
Maprs398124057
PheGenIrs398124057
hapmaprs398124057
1000 genomesrs398124057
hgdprs398124057
ensemblrs398124057
gopubmedrs398124057
geneviewrs398124057
scholarrs398124057
googlers398124057
pharmgkbrs398124057
gwascentralrs398124057
openSNPrs398124057
23andMers398124057
23andMe allrs398124057
SNP Nexus

SNPshotrs398124057
SNPdbers398124057
MSV3drs398124057
GWAS Ctlgrs398124057
Max Magnitude0
ClinVar
Risk rs398124057(;)
Alt rs398124057(;)
Reference rs398124057(G;G)
Significance Pathogenic
Disease Dilated cardiomyopathy 3B
Variation info
Gene DMD
CLNDBN Dilated cardiomyopathy 3B
Reversed 1
HGVS NC_000023.10:g.31697510delC
CLNSRC ClinVar
CLNACC RCV000080773.3,