Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs1801483
rs1801483
0.100 GeneticVariation BEFREE In a combined French-Sardinian study of GCR , there is an association of Gly 40 Ser mutation with T2DM, confirmed by a UK study but not by others. 15931615

2005

dbSNP: rs1801483
rs1801483
0.100 GeneticVariation BEFREE Our results show that the Gly40Ser mutation in the glucagon receptor gene is not associated with type 2 diabetes in a Brazilian population. 11961492

2002

dbSNP: rs1801483
rs1801483
0.100 GeneticVariation BEFREE Our results demonstrate a strong genetic heterogeneity among the ethnic group and suggest that the Gly40Ser mutation of the glucagon receptor gene plays little role, if any, in the pathogenesis of type 2 diabetes and essential hypertension in the Taiwanese population. 10090412

1999

dbSNP: rs1801483
rs1801483
0.100 GeneticVariation BEFREE Although the frequency of the Gly40Ser polymorphism in NIDDM observed in France is not confirmed in our population, this genetic variance is also evident in Germany. 10510728

1999

dbSNP: rs1801483
rs1801483
0.100 GeneticVariation BEFREE In conclusion, our results indicate that the Gly40Ser variation is not associated with NIDDM in the Sardinian population and that its frequency varies in different parts of Sardinia. 9028723

1997

dbSNP: rs1801483
rs1801483
0.100 GeneticVariation BEFREE Our results suggest that Gly40Ser polymorphism of the GCG-R gene is not associated with NIDDM in the Russian population and point to the genetic heterogeneity of NIDDM in different ethnic groups. 9285210

1997

dbSNP: rs1801483
rs1801483
0.100 GeneticVariation BEFREE Restricted geographical extension of the association of a glucagon receptor gene mutation (Gly40Ser) with non-insulin-dependent diabetes mellitus. 8858207

1996

dbSNP: rs1801483
rs1801483
0.100 GeneticVariation BEFREE We have previously reported that a single heterozygous missense mutation in exon 2 of the glucagon receptor gene, which changes a glycine to a serine (Gly40Ser), is associated with NIDDM in a French population. 8635644

1996

dbSNP: rs1801483
rs1801483
0.100 GeneticVariation BEFREE Thus, the Gly40-Ser mutation does not play an important role in the pathogenesis of NIDDM in Japanese patients. 8879960

1996

dbSNP: rs1801483
rs1801483
0.100 GeneticVariation BEFREE Absence of association between the Gly40-->Ser mutation in the human glucagon receptor and Japanese patients with non-insulin-dependent diabetes mellitus or impaired glucose tolerance. 8931690

1996

dbSNP: rs1801483
rs1801483
0.100 GeneticVariation BEFREE Recently, subtypes of typical NIDDM were suggested based on missense mutations of mitochondrial DNA [tRNALeu(UUR)] and the glucagon receptor gene (Gly40Ser). 8732719

1996

dbSNP: rs1801483
rs1801483
0.100 GeneticVariation BEFREE None of the Japanese diabetic patients showed Gly40Ser mutation and the association of this mutation with NIDDM was significantly different (p < 4.10(-5) vs French, p < 3.10(-6) vs Sardinian by Fisher's exact test). 7589886

1995

dbSNP: rs1801483
rs1801483
0.100 GeneticVariation BEFREE Taken together, the data do not support the suggested involvement of the Gly40Ser polymorphism in impaired glucose tolerance and the hypothesis of an association between NIDDM and the glucagon receptor gene in this population. 8690179

1995