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rs398123856

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(;) 0 common in clinvar
Make rs398123856(-;-)
Make rs398123856(-;AG)
Make rs398123856(AG;AG)
ReferenceGRCh38 38.1/141
ChromosomeX
Position32614442
GeneDMD
is asnp
is mentioned by
dbSNPrs398123856
ebirs398123856
HLIrs398123856
Exacrs398123856
Varsomers398123856
Maprs398123856
PheGenIrs398123856
hapmaprs398123856
1000 genomesrs398123856
hgdprs398123856
ensemblrs398123856
gopubmedrs398123856
geneviewrs398123856
scholarrs398123856
googlers398123856
pharmgkbrs398123856
gwascentralrs398123856
openSNPrs398123856
23andMers398123856
23andMe allrs398123856
SNP Nexus

SNPshotrs398123856
SNPdbers398123856
MSV3drs398123856
GWAS Ctlgrs398123856
Max Magnitude0
ClinVar
Risk rs398123856(AG;AG)
Alt rs398123856(AG;AG)
Reference rs398123856(;)
Significance Pathogenic
Disease Dilated cardiomyopathy 3B Becker muscular dystrophy Duchenne muscular dystrophy
Variation info
Gene DMD
CLNDBN Dilated cardiomyopathy 3B Becker muscular dystrophy Duchenne muscular dystrophy
Reversed 1
HGVS NC_000023.10:g.32632560_32632561dupCT
CLNSRC ClinVar
CLNACC RCV000080447.3, RCV000174324.1, RCV000174325.1,