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rs794727749

From SNPedia

Orientationminus
Make rs794727749(-;-)
Make rs794727749(-;C)
ReferenceGRCh38.p2 38.2/147
ChromosomeX
Position31774058
GeneDMD
is asnp
is mentioned by
dbSNPrs794727749
ebirs794727749
HLIrs794727749
Exacrs794727749
Varsomers794727749
Maprs794727749
PheGenIrs794727749
hapmaprs794727749
1000 genomesrs794727749
hgdprs794727749
ensemblrs794727749
gopubmedrs794727749
geneviewrs794727749
scholarrs794727749
googlers794727749
pharmgkbrs794727749
gwascentralrs794727749
openSNPrs794727749
23andMers794727749
23andMe allrs794727749
SNP Nexus

SNPshotrs794727749
SNPdbers794727749
MSV3drs794727749
GWAS Ctlgrs794727749
Max Magnitude
ClinVar
Risk rs794727749(;)
Alt rs794727749(;)
Reference rs794727749(C;C)
Significance Pathogenic
Disease Becker muscular dystrophy Duchenne muscular dystrophy
Variation info
Gene DMD
CLNDBN Becker muscular dystrophy Duchenne muscular dystrophy
Reversed 1
HGVS NC_000023.10:g.31792175delG
CLNSRC
CLNACC RCV000179091.1, RCV000179092.1,