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

rs398123839

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs398123839(-;-)
Make rs398123839(-;T)
ReferenceGRCh38 38.1/141
ChromosomeX
Position31169542
GeneDMD
is asnp
is mentioned by
dbSNPrs398123839
ebirs398123839
HLIrs398123839
Exacrs398123839
Varsomers398123839
Maprs398123839
PheGenIrs398123839
hapmaprs398123839
1000 genomesrs398123839
hgdprs398123839
ensemblrs398123839
gopubmedrs398123839
geneviewrs398123839
scholarrs398123839
googlers398123839
pharmgkbrs398123839
gwascentralrs398123839
openSNPrs398123839
23andMers398123839
23andMe allrs398123839
SNP Nexus

SNPshotrs398123839
SNPdbers398123839
MSV3drs398123839
GWAS Ctlgrs398123839
Max Magnitude0
ClinVar
Risk rs398123839(;)
Alt rs398123839(;)
Reference rs398123839(T;T)
Significance Pathogenic
Disease Duchenne muscular dystrophy
Variation info
Gene DMD
CLNDBN Duchenne muscular dystrophy
Reversed 1
HGVS NC_000023.10:g.31187659delA
CLNSRC HGMD
CLNACC RCV000080421.4,