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rs398123955

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(;) 0 common in clinvar
Make rs398123955(-;-)
Make rs398123955(-;GTCT)
Make rs398123955(GTCT;GTCT)
ReferenceGRCh38 38.1/141
ChromosomeX
Position32389606
GeneDMD
is asnp
is mentioned by
dbSNPrs398123955
ebirs398123955
HLIrs398123955
Exacrs398123955
Varsomers398123955
Maprs398123955
PheGenIrs398123955
hapmaprs398123955
1000 genomesrs398123955
hgdprs398123955
ensemblrs398123955
gopubmedrs398123955
geneviewrs398123955
scholarrs398123955
googlers398123955
pharmgkbrs398123955
gwascentralrs398123955
openSNPrs398123955
23andMers398123955
23andMe allrs398123955
SNP Nexus

SNPshotrs398123955
SNPdbers398123955
MSV3drs398123955
GWAS Ctlgrs398123955
Max Magnitude0
ClinVar
Risk rs398123955(GTCT;GTCT)
Alt rs398123955(GTCT;GTCT)
Reference rs398123955(;)
Significance Pathogenic
Disease Dilated cardiomyopathy 3B
Variation info
Gene DMD
CLNDBN Dilated cardiomyopathy 3B
Reversed 1
HGVS NC_000023.10:g.32407724_32407727dupAGAC
CLNSRC ClinVar
CLNACC RCV000080615.3,