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rs398124052

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs398124052(A;A)
Make rs398124052(A;G)
ReferenceGRCh38 38.1/141
ChromosomeX
Position31679565
GeneDMD
is asnp
is mentioned by
dbSNPrs398124052
ebirs398124052
HLIrs398124052
Exacrs398124052
Varsomers398124052
Maprs398124052
PheGenIrs398124052
hapmaprs398124052
1000 genomesrs398124052
hgdprs398124052
ensemblrs398124052
gopubmedrs398124052
geneviewrs398124052
scholarrs398124052
googlers398124052
pharmgkbrs398124052
gwascentralrs398124052
openSNPrs398124052
23andMers398124052
23andMe allrs398124052
SNP Nexus

SNPshotrs398124052
SNPdbers398124052
MSV3drs398124052
GWAS Ctlgrs398124052
Max Magnitude0
ClinVar
Risk rs398124052(A;A)
Alt rs398124052(A;A)
Reference rs398124052(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.31697682C>T
CLNSRC HGMD
CLNACC RCV000080767.4, RCV000179125.1, RCV000179126.1,