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rs398123921

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs398123921(A;A)
Make rs398123921(A;G)
ReferenceGRCh38 38.1/141
ChromosomeX
Position32468573
GeneDMD
is asnp
is mentioned by
dbSNPrs398123921
ebirs398123921
HLIrs398123921
Exacrs398123921
Varsomers398123921
Maprs398123921
PheGenIrs398123921
hapmaprs398123921
1000 genomesrs398123921
hgdprs398123921
ensemblrs398123921
gopubmedrs398123921
geneviewrs398123921
scholarrs398123921
googlers398123921
pharmgkbrs398123921
gwascentralrs398123921
openSNPrs398123921
23andMers398123921
23andMe allrs398123921
SNP Nexus

SNPshotrs398123921
SNPdbers398123921
MSV3drs398123921
GWAS Ctlgrs398123921
Max Magnitude0
ClinVar
Risk rs398123921(A,C;A,C)
Alt rs398123921(A,C;A,C)
Reference rs398123921(G;G)
Significance Pathogenic
Disease Dilated cardiomyopathy 3B
Variation info
Gene DMD
CLNDBN Dilated cardiomyopathy 3B
Reversed 1
HGVS NC_000023.10:g.32486690C>T
CLNSRC HGMD
CLNACC RCV000080540.3,