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rs398123864

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(CTC;CTC) 0 common in clinvar
Make rs398123864(-;-)
Make rs398123864(-;CTC)
ReferenceGRCh38 38.1/141
ChromosomeX
Position32849752
GeneDMD
is asnp
is mentioned by
dbSNPrs398123864
ebirs398123864
HLIrs398123864
Exacrs398123864
Varsomers398123864
Maprs398123864
PheGenIrs398123864
hapmaprs398123864
1000 genomesrs398123864
hgdprs398123864
ensemblrs398123864
gopubmedrs398123864
geneviewrs398123864
scholarrs398123864
googlers398123864
pharmgkbrs398123864
gwascentralrs398123864
openSNPrs398123864
23andMers398123864
23andMe allrs398123864
SNP Nexus

SNPshotrs398123864
SNPdbers398123864
MSV3drs398123864
GWAS Ctlgrs398123864
Max Magnitude0
ClinVar
Risk rs398123864(;)
Alt rs398123864(;)
Reference rs398123864(CTC;CTC)
Significance Pathogenic
Disease Dilated cardiomyopathy 3B
Variation info
Gene DMD
CLNDBN Dilated cardiomyopathy 3B
Reversed 1
HGVS NC_000023.10:g.32867869_32867871delGAG
CLNSRC HGMD
CLNACC RCV000080460.3,