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rs398123945

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs398123945(-;-)
Make rs398123945(-;G)
ReferenceGRCh38 38.1/141
ChromosomeX
Position32448495
GeneDMD
is asnp
is mentioned by
dbSNPrs398123945
ebirs398123945
HLIrs398123945
Exacrs398123945
Varsomers398123945
Maprs398123945
PheGenIrs398123945
hapmaprs398123945
1000 genomesrs398123945
hgdprs398123945
ensemblrs398123945
gopubmedrs398123945
geneviewrs398123945
scholarrs398123945
googlers398123945
pharmgkbrs398123945
gwascentralrs398123945
openSNPrs398123945
23andMers398123945
23andMe allrs398123945
SNP Nexus

SNPshotrs398123945
SNPdbers398123945
MSV3drs398123945
GWAS Ctlgrs398123945
Max Magnitude0
ClinVar
Risk rs398123945(;)
Alt rs398123945(;)
Reference rs398123945(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.32466612delC
CLNSRC ClinVar
CLNACC RCV000080594.4, RCV000176743.1, RCV000176744.1,