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rs398123987

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(;) 0 common in clinvar
Make rs398123987(-;-)
Make rs398123987(-;T)
Make rs398123987(T;T)
ReferenceGRCh38 38.1/141
ChromosomeX
Position32362799
GeneDMD
is asnp
is mentioned by
dbSNPrs398123987
ebirs398123987
HLIrs398123987
Exacrs398123987
Varsomers398123987
Maprs398123987
PheGenIrs398123987
hapmaprs398123987
1000 genomesrs398123987
hgdprs398123987
ensemblrs398123987
gopubmedrs398123987
geneviewrs398123987
scholarrs398123987
googlers398123987
pharmgkbrs398123987
gwascentralrs398123987
openSNPrs398123987
23andMers398123987
23andMe allrs398123987
SNP Nexus

SNPshotrs398123987
SNPdbers398123987
MSV3drs398123987
GWAS Ctlgrs398123987
Max Magnitude0
ClinVar
Risk rs398123987(T;T)
Alt rs398123987(T;T)
Reference rs398123987(;)
Significance Pathogenic
Disease Dilated cardiomyopathy 3B
Variation info
Gene DMD
CLNDBN Dilated cardiomyopathy 3B
Reversed 1
HGVS NC_000023.10:g.32380917dupA
CLNSRC ClinVar
CLNACC RCV000080654.3,