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rs398123901

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs398123901(A;A)
Make rs398123901(A;G)
ReferenceGRCh38 38.1/141
ChromosomeX
Position32491276
GeneDMD
is asnp
is mentioned by
dbSNPrs398123901
ClinGenrs398123901
ebirs398123901
HLIrs398123901
Exacrs398123901
Varsomers398123901
Maprs398123901
PheGenIrs398123901
hapmaprs398123901
1000 genomesrs398123901
hgdprs398123901
ensemblrs398123901
gopubmedrs398123901
geneviewrs398123901
scholarrs398123901
googlers398123901
pharmgkbrs398123901
gwascentralrs398123901
openSNPrs398123901
23andMers398123901
23andMe allrs398123901
SNP Nexus

SNPshotrs398123901
SNPdbers398123901
MSV3drs398123901
GWAS Ctlgrs398123901
Max Magnitude0
ClinVar
Risk rs398123901(A;A)
Alt rs398123901(A;A)
Reference Rs398123901(G;G)
Significance Pathogenic
Disease Dilated cardiomyopathy 3B
Variation info
Gene DMD
CLNDBN Dilated cardiomyopathy 3B
Reversed 1
HGVS NC_000023.10:g.32509393C>T
CLNSRC HGMD
CLNACC RCV000080514.3,