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rs398124076

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs398124076(A;A)
Make rs398124076(A;G)
ReferenceGRCh38 38.1/141
ChromosomeX
Position31478983
GeneDMD
is asnp
is mentioned by
dbSNPrs398124076
ebirs398124076
HLIrs398124076
Exacrs398124076
Varsomers398124076
Maprs398124076
PheGenIrs398124076
hapmaprs398124076
1000 genomesrs398124076
hgdprs398124076
ensemblrs398124076
gopubmedrs398124076
geneviewrs398124076
scholarrs398124076
googlers398124076
pharmgkbrs398124076
gwascentralrs398124076
openSNPrs398124076
23andMers398124076
23andMe allrs398124076
SNP Nexus

SNPshotrs398124076
SNPdbers398124076
MSV3drs398124076
GWAS Ctlgrs398124076
Max Magnitude0
ClinVar
Risk rs398124076(A;A)
Alt rs398124076(A;A)
Reference rs398124076(G;G)
Significance Pathogenic
Disease Dilated cardiomyopathy 3B
Variation info
Gene DMD
CLNDBN Dilated cardiomyopathy 3B
Reversed 1
HGVS NC_000023.10:g.31497100C>T
CLNSRC ClinVar
CLNACC RCV000080808.3,