Have questions? Visit https://www.reddit.com/r/SNPedia

rs398123844

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs398123844(-;-)
Make rs398123844(-;C)
ReferenceGRCh38 38.1/141
ChromosomeX
Position31147447
GeneDMD
is asnp
is mentioned by
dbSNPrs398123844
ebirs398123844
HLIrs398123844
Exacrs398123844
Varsomers398123844
Maprs398123844
PheGenIrs398123844
hapmaprs398123844
1000 genomesrs398123844
hgdprs398123844
ensemblrs398123844
gopubmedrs398123844
geneviewrs398123844
scholarrs398123844
googlers398123844
pharmgkbrs398123844
gwascentralrs398123844
openSNPrs398123844
23andMers398123844
23andMe allrs398123844
SNP Nexus

SNPshotrs398123844
SNPdbers398123844
MSV3drs398123844
GWAS Ctlgrs398123844
Max Magnitude0
ClinVar
Risk rs398123844(;)
Alt rs398123844(;)
Reference rs398123844(C;C)
Significance Pathogenic
Disease Dilated cardiomyopathy 3B
Variation info
Gene DMD
CLNDBN Dilated cardiomyopathy 3B
Reversed 1
HGVS NC_000023.10:g.31165564delG
CLNSRC ClinVar
CLNACC RCV000080428.3,