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rs398123959

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs398123959(-;-)
Make rs398123959(-;A)
ReferenceGRCh38 38.1/141
ChromosomeX
Position32389519
GeneDMD
is asnp
is mentioned by
dbSNPrs398123959
ebirs398123959
HLIrs398123959
Exacrs398123959
Varsomers398123959
Maprs398123959
PheGenIrs398123959
hapmaprs398123959
1000 genomesrs398123959
hgdprs398123959
ensemblrs398123959
gopubmedrs398123959
geneviewrs398123959
scholarrs398123959
googlers398123959
pharmgkbrs398123959
gwascentralrs398123959
openSNPrs398123959
23andMers398123959
23andMe allrs398123959
SNP Nexus

SNPshotrs398123959
SNPdbers398123959
MSV3drs398123959
GWAS Ctlgrs398123959
Max Magnitude0
ClinVar
Risk rs398123959(;)
Alt rs398123959(;)
Reference rs398123959(A;A)
Significance Pathogenic
Disease Dilated cardiomyopathy 3B
Variation info
Gene DMD
CLNDBN Dilated cardiomyopathy 3B
Reversed 1
HGVS NC_000023.10:g.32407636delT
CLNSRC ClinVar
CLNACC RCV000080619.3,