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rs794727322

From SNPedia

Orientationminus
Make rs794727322(-;-)
Make rs794727322(-;AA)
ReferenceGRCh38.p2 38.2/147
ChromosomeX
Position32491297
GeneDMD
is asnp
is mentioned by
dbSNPrs794727322
ebirs794727322
HLIrs794727322
Exacrs794727322
Varsomers794727322
Maprs794727322
PheGenIrs794727322
hapmaprs794727322
1000 genomesrs794727322
hgdprs794727322
ensemblrs794727322
gopubmedrs794727322
geneviewrs794727322
scholarrs794727322
googlers794727322
pharmgkbrs794727322
gwascentralrs794727322
openSNPrs794727322
23andMers794727322
23andMe allrs794727322
SNP Nexus

SNPshotrs794727322
SNPdbers794727322
MSV3drs794727322
GWAS Ctlgrs794727322
Max Magnitude
ClinVar
Risk rs794727322(;)
Alt rs794727322(;)
Reference rs794727322(AA;AA)
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.32509414_32509415delTT
CLNSRC
CLNACC RCV000176068.1, RCV000176069.1,