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rs398124036

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs398124036(A;A)
Make rs398124036(A;G)
ReferenceGRCh38 38.1/141
ChromosomeX
Position31929602
GeneDMD
is asnp
is mentioned by
dbSNPrs398124036
ebirs398124036
HLIrs398124036
Exacrs398124036
Varsomers398124036
Maprs398124036
PheGenIrs398124036
hapmaprs398124036
1000 genomesrs398124036
hgdprs398124036
ensemblrs398124036
gopubmedrs398124036
geneviewrs398124036
scholarrs398124036
googlers398124036
pharmgkbrs398124036
gwascentralrs398124036
openSNPrs398124036
23andMers398124036
23andMe allrs398124036
SNP Nexus

SNPshotrs398124036
SNPdbers398124036
MSV3drs398124036
GWAS Ctlgrs398124036
Max Magnitude0
ClinVar
Risk rs398124036(A,T;A,T)
Alt rs398124036(A,T;A,T)
Reference rs398124036(G;G)
Significance Pathogenic
Disease not provided Dilated cardiomyopathy 3B Becker muscular dystrophy Duchenne muscular dystrophy
Variation info
Gene DMD
CLNDBN not provided Dilated cardiomyopathy 3B Becker muscular dystrophy Duchenne muscular dystrophy
Reversed 1
HGVS NC_000023.10:g.31947719C>A; NC_000023.10:g.31947719C>T
CLNSRC HGMD
CLNACC RCV000178628.1, RCV000080743.4, RCV000178629.1, RCV000178630.1,