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rs398123977

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs398123977(-;-)
Make rs398123977(-;T)
ReferenceGRCh38 38.1/141
ChromosomeX
Position32364684
GeneDMD
is asnp
is mentioned by
dbSNPrs398123977
ebirs398123977
HLIrs398123977
Exacrs398123977
Varsomers398123977
Maprs398123977
PheGenIrs398123977
hapmaprs398123977
1000 genomesrs398123977
hgdprs398123977
ensemblrs398123977
gopubmedrs398123977
geneviewrs398123977
scholarrs398123977
googlers398123977
pharmgkbrs398123977
gwascentralrs398123977
openSNPrs398123977
23andMers398123977
23andMe allrs398123977
SNP Nexus

SNPshotrs398123977
SNPdbers398123977
MSV3drs398123977
GWAS Ctlgrs398123977
Max Magnitude0
ClinVar
Risk rs398123977(;)
Alt rs398123977(;)
Reference rs398123977(T;T)
Significance Pathogenic
Disease Dilated cardiomyopathy 3B
Variation info
Gene DMD
CLNDBN Dilated cardiomyopathy 3B
Reversed 1
HGVS NC_000023.10:g.32382801delA
CLNSRC ClinVar
CLNACC RCV000080641.3,