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rs794726994

From SNPedia

Orientationminus
Make rs794726994(-;-)
Make rs794726994(-;C)
ReferenceGRCh38.p2 38.2/147
ChromosomeX
Position32645043
GeneDMD
is asnp
is mentioned by
dbSNPrs794726994
ebirs794726994
HLIrs794726994
Exacrs794726994
Varsomers794726994
Maprs794726994
PheGenIrs794726994
hapmaprs794726994
1000 genomesrs794726994
hgdprs794726994
ensemblrs794726994
gopubmedrs794726994
geneviewrs794726994
scholarrs794726994
googlers794726994
pharmgkbrs794726994
gwascentralrs794726994
openSNPrs794726994
23andMers794726994
23andMe allrs794726994
SNP Nexus

SNPshotrs794726994
SNPdbers794726994
MSV3drs794726994
GWAS Ctlgrs794726994
Max Magnitude
ClinVar
Risk rs794726994(;)
Alt rs794726994(;)
Reference rs794726994(C;C)
Significance Pathogenic
Disease Becker muscular dystrophy Duchenne muscular dystrophy Dilated cardiomyopathy 3B
Variation info
Gene DMD
CLNDBN Becker muscular dystrophy Duchenne muscular dystrophy Dilated cardiomyopathy 3B
Reversed 1
HGVS NC_000023.10:g.32663160delG
CLNSRC
CLNACC RCV000173791.1, RCV000173792.1, RCV000173793.1,