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rs398122853

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs398122853(A;A)
Make rs398122853(A;G)
ReferenceGRCh38 38.1/141
ChromosomeX
Position33211304
GeneDMD
is asnp
is mentioned by
dbSNPrs398122853
ebirs398122853
HLIrs398122853
Exacrs398122853
Varsomers398122853
Maprs398122853
PheGenIrs398122853
hapmaprs398122853
1000 genomesrs398122853
hgdprs398122853
ensemblrs398122853
gopubmedrs398122853
geneviewrs398122853
scholarrs398122853
googlers398122853
pharmgkbrs398122853
gwascentralrs398122853
openSNPrs398122853
23andMers398122853
23andMe allrs398122853
SNP Nexus

SNPshotrs398122853
SNPdbers398122853
MSV3drs398122853
GWAS Ctlgrs398122853
Max Magnitude0
ClinVar
Risk rs398122853(A;A)
Alt rs398122853(A;A)
Reference rs398122853(G;G)
Significance Pathogenic
Disease Becker muscular dystrophy Dilated cardiomyopathy 3B Duchenne muscular dystrophy not provided
Variation info
Gene DMD
CLNDBN Becker muscular dystrophy Dilated cardiomyopathy 3B Duchenne muscular dystrophy not provided
Reversed 1
HGVS NC_000023.10:g.33229421C>T
CLNSRC HGMD OMIM Allelic Variant
CLNACC RCV000022854.18, RCV000150072.3, RCV000173322.2, RCV000183395.1,