Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs1972863
rs1972863
Entrez Id: 2895
Gene Symbol: GRID2
GRID2
CUI: C0021704
Disease:
Intelligence 		A 0.700 GeneticVariation GWASCAT A combined analysis of genetically correlated traits identifies 187 loci and a role for neurogenesis and myelination in intelligence. 29326435 2019
dbSNP: rs2870710
rs2870710
Entrez Id: 2895
Gene Symbol: GRID2
GRID2
CUI: C1305855
Disease:
Body mass index 		C 0.700 GeneticVariation GWASCAT Meta-analysis of genome-wide association studies for body fat distribution in 694 649 individuals of European ancestry. 30239722 2019
dbSNP: rs4693327
rs4693327
Entrez Id: 2895
Gene Symbol: GRID2
GRID2
CUI: C1305855
Disease:
Body mass index 		0.700 GeneticVariation GWASCAT Leveraging Polygenic Functional Enrichment to Improve GWAS Power. 30595370 2019
dbSNP: rs1972860
rs1972860
Entrez Id: 2895
Gene Symbol: GRID2
GRID2
CUI: C0021704
Disease:
Intelligence 		A 0.700 GeneticVariation GWASCAT Genome-wide association meta-analysis in 269,867 individuals identifies new genetic and functional links to intelligence. 29942086 2018
dbSNP: rs1972863
rs1972863
Entrez Id: 2895
Gene Symbol: GRID2
GRID2
CUI: C0596887
Disease:
mathematical ability 		A 0.700 GeneticVariation GWASCAT Gene discovery and polygenic prediction from a genome-wide association study of educational attainment in 1.1 million individuals. 30038396 2018
dbSNP: rs7655333
rs7655333
Entrez Id: 2895
Gene Symbol: GRID2
GRID2
CUI: C0021704
Disease:
Intelligence 		0.700 GeneticVariation GWASCAT Study of 300,486 individuals identifies 148 independent genetic loci influencing general cognitive function. 29844566 2018
dbSNP: rs17262792
rs17262792
Entrez Id: 2895
Gene Symbol: GRID2
GRID2
CUI: C0006142
Disease:
Malignant neoplasm of breast 		0.700 GeneticVariation GWASDB A locus on 19p13 modifies risk of breast cancer in BRCA1 mutation carriers and is associated with hormone receptor-negative breast cancer in the general population. 20852631 2010
dbSNP: rs368143665
rs368143665
Entrez Id: 2895
Gene Symbol: GRID2
GRID2
CUI: C4015505
Disease:
SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE 18 		A 0.700 GeneticVariation CLINVAR
dbSNP: rs750331613
rs750331613
Entrez Id: 2895
Gene Symbol: GRID2
GRID2
CUI: C0026827
Disease:
Muscle hypotonia 		T 0.700 CausalMutation CLINVAR
dbSNP: rs750331613
rs750331613
Entrez Id: 2895
Gene Symbol: GRID2
GRID2
CUI: C1848207
Disease:
Poor speech 		T 0.700 CausalMutation CLINVAR
dbSNP: rs750331613
rs750331613
Entrez Id: 2895
Gene Symbol: GRID2
GRID2
CUI: C0338656
Disease:
Impaired cognition 		T 0.700 CausalMutation CLINVAR
dbSNP: rs750331613
rs750331613
Entrez Id: 2895
Gene Symbol: GRID2
GRID2
CUI: C0740279
Disease:
Cerebellar atrophy 		T 0.700 CausalMutation CLINVAR
dbSNP: rs750331613
rs750331613
Entrez Id: 2895
Gene Symbol: GRID2
GRID2
CUI: C4015505
Disease:
SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE 18 		T 0.700 CausalMutation CLINVAR
dbSNP: rs1450500
rs1450500
Entrez Id: 2895
Gene Symbol: GRID2
GRID2
CUI: C3714772
Disease:
Recurrent fevers 		0.010 GeneticVariation BEFREE GRID2 gene (4q22.2), encoding for human glutamate receptor delta-2, associated with MKD: The rs1450500 SNP was differently distributed in patients with MKD with respect to those with RF. 25146332 2015
dbSNP: rs1450500
rs1450500
Entrez Id: 2895
Gene Symbol: GRID2
GRID2
CUI: C0342731
Disease:
Deficiency of mevalonate kinase 		0.010 GeneticVariation BEFREE GRID2 gene (4q22.2), encoding for human glutamate receptor delta-2, associated with MKD: The rs1450500 SNP was differently distributed in patients with MKD with respect to those with RF. 25146332 2015