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

rs398124033

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs398124033(A;G)
Make rs398124033(G;G)
ReferenceGRCh38 38.1/141
ChromosomeX
Position31929747
GeneDMD
is asnp
is mentioned by
dbSNPrs398124033
ebirs398124033
HLIrs398124033
Exacrs398124033
Varsomers398124033
Maprs398124033
PheGenIrs398124033
hapmaprs398124033
1000 genomesrs398124033
hgdprs398124033
ensemblrs398124033
gopubmedrs398124033
geneviewrs398124033
scholarrs398124033
googlers398124033
pharmgkbrs398124033
gwascentralrs398124033
openSNPrs398124033
23andMers398124033
23andMe allrs398124033
SNP Nexus

SNPshotrs398124033
SNPdbers398124033
MSV3drs398124033
GWAS Ctlgrs398124033
Max Magnitude0
ClinVar
Risk rs398124033(G;G)
Alt rs398124033(G;G)
Reference rs398124033(A;A)
Significance Pathogenic
Disease Dilated cardiomyopathy 3B
Variation info
Gene DMD
CLNDBN Dilated cardiomyopathy 3B
Reversed 1
HGVS NC_000023.10:g.31947864T>C
CLNSRC ClinVar
CLNACC RCV000080738.3,