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rs398123866

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs398123866(-;-)
Make rs398123866(-;A)
ReferenceGRCh38 38.1/141
ChromosomeX
Position32573608
GeneDMD
is asnp
is mentioned by
dbSNPrs398123866
ebirs398123866
HLIrs398123866
Exacrs398123866
Varsomers398123866
Maprs398123866
PheGenIrs398123866
hapmaprs398123866
1000 genomesrs398123866
hgdprs398123866
ensemblrs398123866
gopubmedrs398123866
geneviewrs398123866
scholarrs398123866
googlers398123866
pharmgkbrs398123866
gwascentralrs398123866
openSNPrs398123866
23andMers398123866
23andMe allrs398123866
SNP Nexus

SNPshotrs398123866
SNPdbers398123866
MSV3drs398123866
GWAS Ctlgrs398123866
Max Magnitude0
ClinVar
Risk rs398123866(;)
Alt rs398123866(;)
Reference rs398123866(A;A)
Significance Pathogenic
Disease Dilated cardiomyopathy 3B
Variation info
Gene DMD
CLNDBN Dilated cardiomyopathy 3B
Reversed 1
HGVS NC_000023.10:g.32591725delT
CLNSRC ClinVar
CLNACC RCV000080465.3,