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rs398124062

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs398124062(-;-)
Make rs398124062(-;C)
ReferenceGRCh38 38.1/141
ChromosomeX
Position31627804
GeneDMD
is asnp
is mentioned by
dbSNPrs398124062
ebirs398124062
HLIrs398124062
Exacrs398124062
Varsomers398124062
Maprs398124062
PheGenIrs398124062
hapmaprs398124062
1000 genomesrs398124062
hgdprs398124062
ensemblrs398124062
gopubmedrs398124062
geneviewrs398124062
scholarrs398124062
googlers398124062
pharmgkbrs398124062
gwascentralrs398124062
openSNPrs398124062
23andMers398124062
23andMe allrs398124062
SNP Nexus

SNPshotrs398124062
SNPdbers398124062
MSV3drs398124062
GWAS Ctlgrs398124062
Max Magnitude0
ClinVar
Risk rs398124062(;)
Alt rs398124062(;)
Reference rs398124062(C;C)
Significance Pathogenic
Disease Dilated cardiomyopathy 3B
Variation info
Gene DMD
CLNDBN Dilated cardiomyopathy 3B
Reversed 1
HGVS NC_000023.10:g.31645921delG
CLNSRC HGMD
CLNACC RCV000080780.3,