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rs398123837

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(TC;TC) 0 common in clinvar
Make rs398123837(-;-)
Make rs398123837(-;CT)
Make rs398123837(CT;CT)
ReferenceGRCh38 38.1/141
ChromosomeX
Position31169549
GeneDMD
is asnp
is mentioned by
dbSNPrs398123837
ebirs398123837
HLIrs398123837
Exacrs398123837
Varsomers398123837
Maprs398123837
PheGenIrs398123837
hapmaprs398123837
1000 genomesrs398123837
hgdprs398123837
ensemblrs398123837
gopubmedrs398123837
geneviewrs398123837
scholarrs398123837
googlers398123837
pharmgkbrs398123837
gwascentralrs398123837
openSNPrs398123837
23andMers398123837
23andMe allrs398123837
SNP Nexus

SNPshotrs398123837
SNPdbers398123837
MSV3drs398123837
GWAS Ctlgrs398123837
Max Magnitude0
ClinVar
Risk rs398123837(;)
Alt rs398123837(;)
Reference rs398123837(TC;TC)
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.31187666_31187667delAG
CLNSRC ClinVar
CLNACC RCV000080419.4, RCV000180056.1, RCV000180057.1,