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rs794727097

From SNPedia

Orientationminus
Make rs794727097(-;-)
Make rs794727097(-;TCAC)
ReferenceGRCh38.p2 38.2/147
ChromosomeX
Position32595823
GeneDMD
is asnp
is mentioned by
dbSNPrs794727097
ebirs794727097
HLIrs794727097
Exacrs794727097
Varsomers794727097
Maprs794727097
PheGenIrs794727097
hapmaprs794727097
1000 genomesrs794727097
hgdprs794727097
ensemblrs794727097
gopubmedrs794727097
geneviewrs794727097
scholarrs794727097
googlers794727097
pharmgkbrs794727097
gwascentralrs794727097
openSNPrs794727097
23andMers794727097
23andMe allrs794727097
SNP Nexus

SNPshotrs794727097
SNPdbers794727097
MSV3drs794727097
GWAS Ctlgrs794727097
Max Magnitude
ClinVar
Risk rs794727097(;)
Alt rs794727097(;)
Reference rs794727097(TCAC;TCAC)
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.32613940_32613943delGTGA
CLNSRC
CLNACC RCV000174531.1, RCV000174532.1,