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rs398123914

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(;) 0 common in clinvar
Make rs398123914(-;-)
Make rs398123914(-;C)
Make rs398123914(C;C)
ReferenceGRCh38 38.1/141
ChromosomeX
Position32472183
GeneDMD
is asnp
is mentioned by
dbSNPrs398123914
ebirs398123914
HLIrs398123914
Exacrs398123914
Varsomers398123914
Maprs398123914
PheGenIrs398123914
hapmaprs398123914
1000 genomesrs398123914
hgdprs398123914
ensemblrs398123914
gopubmedrs398123914
geneviewrs398123914
scholarrs398123914
googlers398123914
pharmgkbrs398123914
gwascentralrs398123914
openSNPrs398123914
23andMers398123914
23andMe allrs398123914
SNP Nexus

SNPshotrs398123914
SNPdbers398123914
MSV3drs398123914
GWAS Ctlgrs398123914
Max Magnitude0
ClinVar
Risk rs398123914(C;C)
Alt rs398123914(C;C)
Reference rs398123914(;)
Significance Pathogenic
Disease Dilated cardiomyopathy 3B
Variation info
Gene DMD
CLNDBN Dilated cardiomyopathy 3B
Reversed 1
HGVS NC_000023.10:g.32490301dupG
CLNSRC ClinVar
CLNACC RCV000080532.3,