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

rs794727575

From SNPedia

Orientationminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs794727575(A;G)
Make rs794727575(G;G)
ReferenceGRCh38.p2 38.2/147
ChromosomeX
Position32380682
GeneDMD
is asnp
is mentioned by
dbSNPrs794727575
ebirs794727575
HLIrs794727575
Exacrs794727575
Varsomers794727575
Maprs794727575
PheGenIrs794727575
hapmaprs794727575
1000 genomesrs794727575
hgdprs794727575
ensemblrs794727575
gopubmedrs794727575
geneviewrs794727575
scholarrs794727575
googlers794727575
pharmgkbrs794727575
gwascentralrs794727575
openSNPrs794727575
23andMers794727575
23andMe allrs794727575
SNP Nexus

SNPshotrs794727575
SNPdbers794727575
MSV3drs794727575
GWAS Ctlgrs794727575
Max Magnitude0
ClinVar
Risk rs794727575(G;G)
Alt rs794727575(G;G)
Reference rs794727575(A;A)
Significance Pathogenic
Disease Duchenne muscular dystrophy Becker muscular dystrophy
Variation info
Gene DMD
CLNDBN Duchenne muscular dystrophy Becker muscular dystrophy
Reversed 1
HGVS NC_000023.10:g.32398799T>C
CLNSRC
CLNACC RCV000177779.1, RCV000177780.1,