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rs794726677

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs794726677(A;A)
Make rs794726677(A;G)
ReferenceGRCh38.p2 38.2/146
Chromosome5
Position127420176
GeneMEGF10
is asnp
is mentioned by
dbSNPrs794726677
ebirs794726677
HLIrs794726677
Exacrs794726677
Varsomers794726677
Maprs794726677
PheGenIrs794726677
hapmaprs794726677
1000 genomesrs794726677
hgdprs794726677
ensemblrs794726677
gopubmedrs794726677
geneviewrs794726677
scholarrs794726677
googlers794726677
pharmgkbrs794726677
gwascentralrs794726677
openSNPrs794726677
23andMers794726677
23andMe allrs794726677
SNP Nexus

SNPshotrs794726677
SNPdbers794726677
MSV3drs794726677
GWAS Ctlgrs794726677
Max Magnitude0
ClinVar
Risk rs794726677(A;A)
Alt rs794726677(A;A)
Reference rs794726677(G;G)
Significance Pathogenic
Disease Myopathy
Variation info
Gene MEGF10
CLNDBN Myopathy, areflexia, respiratory distress, and dysphagia, early-onset
Reversed 0
HGVS NC_000005.9:g.126755868G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000023951.4,