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rs398124035

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs398124035(-;-)
Make rs398124035(-;T)
ReferenceGRCh38 38.1/141
ChromosomeX
Position31929674
GeneDMD
is asnp
is mentioned by
dbSNPrs398124035
ebirs398124035
HLIrs398124035
Exacrs398124035
Varsomers398124035
Maprs398124035
PheGenIrs398124035
hapmaprs398124035
1000 genomesrs398124035
hgdprs398124035
ensemblrs398124035
gopubmedrs398124035
geneviewrs398124035
scholarrs398124035
googlers398124035
pharmgkbrs398124035
gwascentralrs398124035
openSNPrs398124035
23andMers398124035
23andMe allrs398124035
SNP Nexus

SNPshotrs398124035
SNPdbers398124035
MSV3drs398124035
GWAS Ctlgrs398124035
Max Magnitude0
ClinVar
Risk rs398124035(;)
Alt rs398124035(;)
Reference rs398124035(T;T)
Significance Pathogenic
Disease Dilated cardiomyopathy 3B
Variation info
Gene DMD
CLNDBN Dilated cardiomyopathy 3B
Reversed 1
HGVS NC_000023.10:g.31947791delA
CLNSRC ClinVar
CLNACC RCV000080741.3,