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rs398124044

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs398124044(A;A)
Make rs398124044(A;G)
ReferenceGRCh38 38.1/141
ChromosomeX
Position31819974
GeneDMD
is asnp
is mentioned by
dbSNPrs398124044
ebirs398124044
HLIrs398124044
Exacrs398124044
Varsomers398124044
Maprs398124044
PheGenIrs398124044
hapmaprs398124044
1000 genomesrs398124044
hgdprs398124044
ensemblrs398124044
gopubmedrs398124044
geneviewrs398124044
scholarrs398124044
googlers398124044
pharmgkbrs398124044
gwascentralrs398124044
openSNPrs398124044
23andMers398124044
23andMe allrs398124044
SNP Nexus

SNPshotrs398124044
SNPdbers398124044
MSV3drs398124044
GWAS Ctlgrs398124044
Max Magnitude0
ClinVar
Risk rs398124044(A;A)
Alt rs398124044(A;A)
Reference rs398124044(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.31838091C>T
CLNSRC HGMD
CLNACC RCV000080753.4, RCV000179070.1, RCV000179071.1,