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

rs398124082

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs398124082(G;T)
Make rs398124082(T;T)
ReferenceGRCh38 38.1/141
ChromosomeX
Position31323659
GeneDMD
is asnp
is mentioned by
dbSNPrs398124082
ebirs398124082
HLIrs398124082
Exacrs398124082
Varsomers398124082
Maprs398124082
PheGenIrs398124082
hapmaprs398124082
1000 genomesrs398124082
hgdprs398124082
ensemblrs398124082
gopubmedrs398124082
geneviewrs398124082
scholarrs398124082
googlers398124082
pharmgkbrs398124082
gwascentralrs398124082
openSNPrs398124082
23andMers398124082
23andMe allrs398124082
SNP Nexus

SNPshotrs398124082
SNPdbers398124082
MSV3drs398124082
GWAS Ctlgrs398124082
Max Magnitude0
ClinVar
Risk rs398124082(C,T;C,T)
Alt rs398124082(C,T;C,T)
Reference rs398124082(G;G)
Significance Pathogenic
Disease Dilated cardiomyopathy 3B Becker muscular dystrophy Duchenne muscular dystrophy
Variation info
Gene DMD
CLNDBN Dilated cardiomyopathy 3B Becker muscular dystrophy Duchenne muscular dystrophy
Reversed 1
HGVS NC_000023.10:g.31341776C>A; NC_000023.10:g.31341776C>G
CLNSRC HGMD
CLNACC RCV000080823.3, RCV000152757.3, RCV000152758.3, RCV000152759.3,