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rs398124106

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs398124106(G;T)
Make rs398124106(T;T)
ReferenceGRCh38 38.1/141
ChromosomeX
Position31182850
GeneDMD
is asnp
is mentioned by
dbSNPrs398124106
ebirs398124106
HLIrs398124106
Exacrs398124106
Varsomers398124106
Maprs398124106
PheGenIrs398124106
hapmaprs398124106
1000 genomesrs398124106
hgdprs398124106
ensemblrs398124106
gopubmedrs398124106
geneviewrs398124106
scholarrs398124106
googlers398124106
pharmgkbrs398124106
gwascentralrs398124106
openSNPrs398124106
23andMers398124106
23andMe allrs398124106
SNP Nexus

SNPshotrs398124106
SNPdbers398124106
MSV3drs398124106
GWAS Ctlgrs398124106
Max Magnitude0
ClinVar
Risk rs398124106(T;T)
Alt rs398124106(T;T)
Reference rs398124106(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.31200967C>A
CLNSRC HGMD
CLNACC RCV000080863.4, RCV000179677.1, RCV000179678.1,