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rs398124100

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs398124100(A;G)
Make rs398124100(G;G)
ReferenceGRCh38 38.1/141
ChromosomeX
Position31204120
GeneDMD
is asnp
is mentioned by
dbSNPrs398124100
ebirs398124100
HLIrs398124100
Exacrs398124100
Varsomers398124100
Maprs398124100
PheGenIrs398124100
hapmaprs398124100
1000 genomesrs398124100
hgdprs398124100
ensemblrs398124100
gopubmedrs398124100
geneviewrs398124100
scholarrs398124100
googlers398124100
pharmgkbrs398124100
gwascentralrs398124100
openSNPrs398124100
23andMers398124100
23andMe allrs398124100
SNP Nexus

SNPshotrs398124100
SNPdbers398124100
MSV3drs398124100
GWAS Ctlgrs398124100
Max Magnitude0
ClinVar
Risk rs398124100(G;G)
Alt rs398124100(G;G)
Reference rs398124100(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.31222237T>C
CLNSRC ClinVar
CLNACC RCV000080854.4, RCV000179670.1, RCV000179671.1,