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

rs398124013

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(;) 0 common in clinvar
Make rs398124013(-;-)
Make rs398124013(-;CA)
Make rs398124013(CA;CA)
ReferenceGRCh38 38.1/141
ChromosomeX
Position32216961
GeneDMD
is asnp
is mentioned by
dbSNPrs398124013
ebirs398124013
HLIrs398124013
Exacrs398124013
Varsomers398124013
Maprs398124013
PheGenIrs398124013
hapmaprs398124013
1000 genomesrs398124013
hgdprs398124013
ensemblrs398124013
gopubmedrs398124013
geneviewrs398124013
scholarrs398124013
googlers398124013
pharmgkbrs398124013
gwascentralrs398124013
openSNPrs398124013
23andMers398124013
23andMe allrs398124013
SNP Nexus

SNPshotrs398124013
SNPdbers398124013
MSV3drs398124013
GWAS Ctlgrs398124013
Max Magnitude0
ClinVar
Risk rs398124013(CA;CA)
Alt rs398124013(CA;CA)
Reference rs398124013(;)
Significance Pathogenic
Disease Dilated cardiomyopathy 3B
Variation info
Gene DMD
CLNDBN Dilated cardiomyopathy 3B
Reversed 1
HGVS NC_000023.10:g.32235078_32235079insTG
CLNSRC ClinVar
CLNACC RCV000080699.3,