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rs398123863

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(TC;TC) 0 common in clinvar
Make rs398123863(-;-)
Make rs398123863(-;TC)
ReferenceGRCh38 38.1/141
ChromosomeX
Position32595829
GeneDMD
is asnp
is mentioned by
dbSNPrs398123863
ebirs398123863
HLIrs398123863
Exacrs398123863
Varsomers398123863
Maprs398123863
PheGenIrs398123863
hapmaprs398123863
1000 genomesrs398123863
hgdprs398123863
ensemblrs398123863
gopubmedrs398123863
geneviewrs398123863
scholarrs398123863
googlers398123863
pharmgkbrs398123863
gwascentralrs398123863
openSNPrs398123863
23andMers398123863
23andMe allrs398123863
SNP Nexus

SNPshotrs398123863
SNPdbers398123863
MSV3drs398123863
GWAS Ctlgrs398123863
Max Magnitude0
ClinVar
Risk rs398123863(;)
Alt rs398123863(;)
Reference rs398123863(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.32613946_32613947delGA
CLNSRC ClinVar
CLNACC RCV000080458.4, RCV000174529.1, RCV000174530.1,