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rs398124080

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs398124080(-;-)
Make rs398124080(-;A)
ReferenceGRCh38 38.1/141
ChromosomeX
Position31348594
GeneDMD
is asnp
is mentioned by
dbSNPrs398124080
ebirs398124080
HLIrs398124080
Exacrs398124080
Varsomers398124080
Maprs398124080
PheGenIrs398124080
hapmaprs398124080
1000 genomesrs398124080
hgdprs398124080
ensemblrs398124080
gopubmedrs398124080
geneviewrs398124080
scholarrs398124080
googlers398124080
pharmgkbrs398124080
gwascentralrs398124080
openSNPrs398124080
23andMers398124080
23andMe allrs398124080
SNP Nexus

SNPshotrs398124080
SNPdbers398124080
MSV3drs398124080
GWAS Ctlgrs398124080
Max Magnitude0
ClinVar
Risk rs398124080(;)
Alt rs398124080(;)
Reference rs398124080(A;A)
Significance Pathogenic
Disease Dilated cardiomyopathy 3B Becker muscular dystrophy Duchenne muscular dystrophy
Variation info
Gene DMD
CLNDBN Dilated cardiomyopathy 3B Becker muscular dystrophy Duchenne muscular dystrophy
Reversed 1
HGVS NC_000023.10:g.31366711delT
CLNSRC ClinVar
CLNACC RCV000080821.4, RCV000179587.1, RCV000179588.1,