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rs794727567

From SNPedia

Orientationminus
Make rs794727567(-;-)
Make rs794727567(-;T)
ReferenceGRCh38.p2 38.2/147
ChromosomeX
Position32386461
GeneDMD
is asnp
is mentioned by
dbSNPrs794727567
ebirs794727567
HLIrs794727567
Exacrs794727567
Varsomers794727567
Maprs794727567
PheGenIrs794727567
hapmaprs794727567
1000 genomesrs794727567
hgdprs794727567
ensemblrs794727567
gopubmedrs794727567
geneviewrs794727567
scholarrs794727567
googlers794727567
pharmgkbrs794727567
gwascentralrs794727567
openSNPrs794727567
23andMers794727567
23andMe allrs794727567
SNP Nexus

SNPshotrs794727567
SNPdbers794727567
MSV3drs794727567
GWAS Ctlgrs794727567
Max Magnitude
ClinVar
Risk rs794727567(;)
Alt rs794727567(;)
Reference rs794727567(T;T)
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.32404578delA
CLNSRC
CLNACC RCV000177739.1, RCV000177740.1,