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rs398124032

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs398124032(A;A)
Make rs398124032(A;G)
ReferenceGRCh38 38.1/141
ChromosomeX
Position32809492
GeneDMD
is asnp
is mentioned by
dbSNPrs398124032
ebirs398124032
HLIrs398124032
Exacrs398124032
Varsomers398124032
Maprs398124032
PheGenIrs398124032
hapmaprs398124032
1000 genomesrs398124032
hgdprs398124032
ensemblrs398124032
gopubmedrs398124032
geneviewrs398124032
scholarrs398124032
googlers398124032
pharmgkbrs398124032
gwascentralrs398124032
openSNPrs398124032
23andMers398124032
23andMe allrs398124032
SNP Nexus

SNPshotrs398124032
SNPdbers398124032
MSV3drs398124032
GWAS Ctlgrs398124032
Max Magnitude0
ClinVar
Risk rs398124032(A;A)
Alt rs398124032(A;A)
Reference rs398124032(G;G)
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.32827609C>T
CLNSRC ClinVar
CLNACC RCV000080736.4, RCV000179876.1, RCV000179877.1,