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rs794727358

From SNPedia

Orientationminus
Make rs794727358(-;-)
Make rs794727358(-;TT)
ReferenceGRCh38.p2 38.2/147
ChromosomeX
Position32472297
GeneDMD
is asnp
is mentioned by
dbSNPrs794727358
ebirs794727358
HLIrs794727358
Exacrs794727358
Varsomers794727358
Maprs794727358
PheGenIrs794727358
hapmaprs794727358
1000 genomesrs794727358
hgdprs794727358
ensemblrs794727358
gopubmedrs794727358
geneviewrs794727358
scholarrs794727358
googlers794727358
pharmgkbrs794727358
gwascentralrs794727358
openSNPrs794727358
23andMers794727358
23andMe allrs794727358
SNP Nexus

SNPshotrs794727358
SNPdbers794727358
MSV3drs794727358
GWAS Ctlgrs794727358
Max Magnitude
ClinVar
Risk rs794727358(;)
Alt rs794727358(;)
Reference rs794727358(TT;TT)
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.32490414_32490415delAA
CLNSRC
CLNACC RCV000176303.1, RCV000176304.1,