Have questions? Visit https://www.reddit.com/r/SNPedia

rs398124055

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs398124055(G;T)
Make rs398124055(T;T)
ReferenceGRCh38 38.1/141
ChromosomeX
Position31679476
GeneDMD
is asnp
is mentioned by
dbSNPrs398124055
dbSNP (classic)rs398124055
ClinGenrs398124055
ebirs398124055
HLIrs398124055
Exacrs398124055
Gnomadrs398124055
Varsomers398124055
LitVarrs398124055
Maprs398124055
PheGenIrs398124055
Biobankrs398124055
1000 genomesrs398124055
hgdprs398124055
ensemblrs398124055
geneviewrs398124055
scholarrs398124055
googlers398124055
pharmgkbrs398124055
gwascentralrs398124055
openSNPrs398124055
23andMers398124055
SNPshotrs398124055
SNPdbers398124055
MSV3drs398124055
GWAS Ctlgrs398124055
Max Magnitude0
ClinVar
Risk rs398124055(T;T)
Alt rs398124055(T;T)
Reference Rs398124055(G;G)
Significance Pathogenic
Disease Dilated cardiomyopathy 3B
Variation info
Gene DMD
CLNDBN Dilated cardiomyopathy 3B
Reversed 1
HGVS NC_000023.10:g.31697593C>A
CLNSRC ClinVar Emory University
CLNACC RCV000080771.3,