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

rs398123908

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs398123908(A;A)
Make rs398123908(A;G)
ReferenceGRCh38 38.1/141
ChromosomeX
Position32484918
GeneDMD
is asnp
is mentioned by
dbSNPrs398123908
ebirs398123908
HLIrs398123908
Exacrs398123908
Varsomers398123908
Maprs398123908
PheGenIrs398123908
hapmaprs398123908
1000 genomesrs398123908
hgdprs398123908
ensemblrs398123908
gopubmedrs398123908
geneviewrs398123908
scholarrs398123908
googlers398123908
pharmgkbrs398123908
gwascentralrs398123908
openSNPrs398123908
23andMers398123908
23andMe allrs398123908
SNP Nexus

SNPshotrs398123908
SNPdbers398123908
MSV3drs398123908
GWAS Ctlgrs398123908
Max Magnitude0
ClinVar
Risk rs398123908(A,T;A,T)
Alt rs398123908(A,T;A,T)
Reference rs398123908(G;G)
Significance Pathogenic
Disease Dilated cardiomyopathy 3B Duchenne muscular dystrophy Becker muscular dystrophy
Variation info
Gene DMD
CLNDBN Dilated cardiomyopathy 3B Duchenne muscular dystrophy Becker muscular dystrophy
Reversed 1
HGVS NC_000023.10:g.32503035C>A; NC_000023.10:g.32503035C>G; NC_000023.10:g.32503035C>T
CLNSRC HGMD
CLNACC RCV000080524.3, RCV000176205.1, RCV000176206.1, RCV000080523.3,