Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs121908631
rs121908631
CLTA ; GNE
0.710 GeneticVariation UNIPROT Novel GNE mutations in Italian families with autosomal recessive hereditary inclusion-body myopathy. 15146476

2004

dbSNP: rs121908631
rs121908631
CLTA ; GNE
0.710 GeneticVariation UNIPROT GNE mutations causing distal myopathy with rimmed vacuoles with inflammation. 12913203

2003

dbSNP: rs121908631
rs121908631
CLTA ; GNE
0.710 GeneticVariation UNIPROT Mutations spectrum of GNE in hereditary inclusion body myopathy sparing the quadriceps. 12497639

2003

dbSNP: rs121908631
rs121908631
CLTA ; GNE
0.710 GeneticVariation UNIPROT Novel missense mutation and large deletion of GNE gene in autosomal-recessive inclusion-body myopathy. 12811782

2003

dbSNP: rs121908631
rs121908631
CLTA ; GNE
0.710 GeneticVariation UNIPROT Sequence and haplotype analyses of GNE in two siblings with Nonaka myopathy from a Japanese family revealed that both patients were compound heterozygotes for a C-->T transition (A460V) in exon 8 and a G-->C transition (V572L) in exon 10. 11916006

2002

dbSNP: rs121908631
rs121908631
CLTA ; GNE
0.710 GeneticVariation UNIPROT Distal myopathy with rimmed vacuoles is allelic to hereditary inclusion body myopathy. 12473753

2002

dbSNP: rs121908631
rs121908631
CLTA ; GNE
0.710 GeneticVariation UNIPROT An Italian family with autosomal recessive inclusion-body myopathy and mutations in the GNE gene. 12473780

2002

dbSNP: rs121908631
rs121908631
CLTA ; GNE
0.710 GeneticVariation BEFREE Sequence and haplotype analyses of GNE in two siblings with Nonaka myopathy from a Japanese family revealed that both patients were compound heterozygotes for a C-->T transition (A460V) in exon 8 and a G-->C transition (V572L) in exon 10. 11916006

2002

dbSNP: rs121908631
rs121908631
CLTA ; GNE
0.710 GeneticVariation UNIPROT Four novel mutations associated with autosomal recessive inclusion body myopathy (MIM: 600737). 12409274

2002

dbSNP: rs121908631
rs121908631
CLTA ; GNE
0.710 GeneticVariation UNIPROT A novel mutation in the GNE gene and a linkage disequilibrium in Japanese pedigrees. 12325084

2002

dbSNP: rs121908631
rs121908631
CLTA ; GNE
0.710 GeneticVariation UNIPROT Distal myopathy with rimmed vacuoles: novel mutations in the GNE gene. 12177386

2002

dbSNP: rs121908631
rs121908631
CLTA ; GNE
0.710 GeneticVariation UNIPROT GNE mutations in an American family with quadriceps-sparing IBM and lack of mutations in s-IBM. 12473769

2002

dbSNP: rs121908631
rs121908631
CLTA ; GNE
0.710 GeneticVariation UNIPROT The UDP-N-acetylglucosamine 2-epimerase/N-acetylmannosamine kinase gene is mutated in recessive hereditary inclusion body myopathy. 11528398

2001