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rs398123957

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(AA;AA) 0 common in clinvar
Make rs398123957(-;-)
Make rs398123957(-;AA)
ReferenceGRCh38 38.1/141
ChromosomeX
Position32389547
GeneDMD
is asnp
is mentioned by
dbSNPrs398123957
ebirs398123957
HLIrs398123957
Exacrs398123957
Varsomers398123957
Maprs398123957
PheGenIrs398123957
hapmaprs398123957
1000 genomesrs398123957
hgdprs398123957
ensemblrs398123957
gopubmedrs398123957
geneviewrs398123957
scholarrs398123957
googlers398123957
pharmgkbrs398123957
gwascentralrs398123957
openSNPrs398123957
23andMers398123957
23andMe allrs398123957
SNP Nexus

SNPshotrs398123957
SNPdbers398123957
MSV3drs398123957
GWAS Ctlgrs398123957
Max Magnitude0
ClinVar
Risk rs398123957(;)
Alt rs398123957(;)
Reference rs398123957(AA;AA)
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.32407664_32407665delTT
CLNSRC HGMD
CLNACC RCV000080617.4, RCV000177649.1, RCV000177650.1,