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rs773729410

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs773729410(A;A)
Make rs773729410(A;G)
ReferenceGRCh38.p2 38.2/146
Chromosome9
Position36236865
GeneGNE
is asnp
is mentioned by
dbSNPrs773729410
ebirs773729410
HLIrs773729410
Exacrs773729410
Varsomers773729410
Maprs773729410
PheGenIrs773729410
hapmaprs773729410
1000 genomesrs773729410
hgdprs773729410
ensemblrs773729410
gopubmedrs773729410
geneviewrs773729410
scholarrs773729410
googlers773729410
pharmgkbrs773729410
gwascentralrs773729410
openSNPrs773729410
23andMers773729410
23andMe allrs773729410
SNP Nexus

SNPshotrs773729410
SNPdbers773729410
MSV3drs773729410
GWAS Ctlgrs773729410
Max Magnitude0
ClinVar
Risk rs773729410(A;A)
Alt rs773729410(A;A)
Reference rs773729410(G;G)
Significance Pathogenic
Disease Inclusion body myopathy 2
Variation info
Gene GNE
CLNDBN Inclusion body myopathy 2
Reversed 0
HGVS NC_000009.11:g.36236862G>A
CLNSRC
CLNACC RCV000178150.1,