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

rs398123877

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(TAG;TAG) 0 common in clinvar
Make rs398123877(AA;AA)
Make rs398123877(AA;TAG)
ReferenceGRCh38 38.1/141
ChromosomeX
Position32518132
GeneDMD
is asnp
is mentioned by
dbSNPrs398123877
ebirs398123877
HLIrs398123877
Exacrs398123877
Varsomers398123877
Maprs398123877
PheGenIrs398123877
hapmaprs398123877
1000 genomesrs398123877
hgdprs398123877
ensemblrs398123877
gopubmedrs398123877
geneviewrs398123877
scholarrs398123877
googlers398123877
pharmgkbrs398123877
gwascentralrs398123877
openSNPrs398123877
23andMers398123877
23andMe allrs398123877
SNP Nexus

SNPshotrs398123877
SNPdbers398123877
MSV3drs398123877
GWAS Ctlgrs398123877
Max Magnitude0
ClinVar
Risk rs398123877(AA;AA)
Alt rs398123877(AA;AA)
Reference rs398123877(TAG;TAG)
Significance Pathogenic
Disease Dilated cardiomyopathy 3B
Variation info
Gene DMD
CLNDBN Dilated cardiomyopathy 3B
Reversed 1
HGVS NC_000023.10:g.32536249_32536251delCTAinsTT
CLNSRC
CLNACC RCV000080483.3,