DLG2, discs large MAGUK scaffold protein 2, 1740

N. diseases: 44; N. variants: 28
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs11823251
rs11823251
Entrez Id: 1740
Gene Symbol: DLG2
DLG2
CUI: C1314691
Disease:
Age at menarche 		0.700 GeneticVariation GWASCAT Leveraging Polygenic Functional Enrichment to Improve GWAS Power. 30595370 2019
dbSNP: rs349071
rs349071
Entrez Id: 1740
Gene Symbol: DLG2
DLG2
CUI: C1305855
Disease:
Body mass index 		0.700 GeneticVariation GWASCAT Leveraging Polygenic Functional Enrichment to Improve GWAS Power. 30595370 2019
dbSNP: rs349071
rs349071
Entrez Id: 1740
Gene Symbol: DLG2
DLG2
CUI: C1305855
Disease:
Body mass index 		A 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: rs349088
rs349088
Entrez Id: 1740
Gene Symbol: DLG2
DLG2
CUI: C1305855
Disease:
Body mass index 		A 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: rs536665
rs536665
Entrez Id: 1740
Gene Symbol: DLG2
DLG2
CUI: C0205682
Disease:
Waist-Hip Ratio 		A 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: rs17807909
rs17807909
Entrez Id: 1740
Gene Symbol: DLG2
DLG2
CUI: C2076600
Disease:
Influenza due to Influenza A virus subtype H1N1 		0.700 GeneticVariation GWASCAT No Major Host Genetic Risk Factor Contributed to A(H1N1)2009 Influenza Severity. 26379185 2015
dbSNP: rs10466716
rs10466716
Entrez Id: 1740;101929043
Gene Symbol: DLG2;DLG2-AS2
DLG2;DLG2-AS2
CUI: C0410702
Disease:
Adolescent idiopathic scoliosis 		0.700 GeneticVariation GWASCAT The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease. 30019117 2018
dbSNP: rs10466716
rs10466716
Entrez Id: 1740;101929043
Gene Symbol: DLG2;DLG2-AS2
DLG2;DLG2-AS2
CUI: C1837461
Disease:
SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3 		0.700 GeneticVariation GWASCAT The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease. 30019117 2018
dbSNP: rs790357
rs790357
Entrez Id: 1740
Gene Symbol: DLG2
DLG2
CUI: C0595921
Disease:
Intraocular pressure disorder 		0.010 GeneticVariation BEFREE The GWAS results revealed a study-wise significant association for IOP at rs790357, which is located within <i>DLG2</i> on chr11q14.1 (p = 1.02×10<sup>-7</sup>). 28966548 2017
dbSNP: rs142615018
rs142615018
Entrez Id: 1740
Gene Symbol: DLG2
DLG2
CUI: C1305855
Disease:
Body mass index 		T 0.700 GeneticVariation GWASCAT Whole-Genome Sequencing Coupled to Imputation Discovers Genetic Signals for Anthropometric Traits. 28552196 2017
dbSNP: rs286028
rs286028
Entrez Id: 1740
Gene Symbol: DLG2
DLG2
CUI: C0005910
Disease:
Body Weight 		A 0.700 GeneticVariation GWASCAT Whole-Genome Sequencing Coupled to Imputation Discovers Genetic Signals for Anthropometric Traits. 28552196 2017