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rs398124091

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs398124091(A;G)
Make rs398124091(G;G)
ReferenceGRCh38 38.1/141
ChromosomeX
Position31261663
GeneDMD
is asnp
is mentioned by
dbSNPrs398124091
ebirs398124091
HLIrs398124091
Exacrs398124091
Varsomers398124091
Maprs398124091
PheGenIrs398124091
hapmaprs398124091
1000 genomesrs398124091
hgdprs398124091
ensemblrs398124091
gopubmedrs398124091
geneviewrs398124091
scholarrs398124091
googlers398124091
pharmgkbrs398124091
gwascentralrs398124091
openSNPrs398124091
23andMers398124091
23andMe allrs398124091
SNP Nexus

SNPshotrs398124091
SNPdbers398124091
MSV3drs398124091
GWAS Ctlgrs398124091
Max Magnitude0
ClinVar
Risk rs398124091(G;G)
Alt rs398124091(G;G)
Reference rs398124091(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.31279780T>C
CLNSRC HGMD
CLNACC RCV000080835.4, RCV000179615.1, RCV000179616.1,