Source: GWASCAT

Gene Disease Score gda Association Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 6934
Gene Symbol: TCF7L2
TCF7L2
CUI: C0011860
Disease: Diabetes Mellitus, Non-Insulin-Dependent
Diabetes Mellitus, Non-Insulin-Dependent 		0.700 GeneticVariation GWASCAT ZRANB3 is an African-specific type 2 diabetes locus associated with beta-cell mass and insulin response. 31324766

2019
Entrez Id: 7054
Gene Symbol: TH
TH
CUI: C0011860
Disease: Diabetes Mellitus, Non-Insulin-Dependent
Diabetes Mellitus, Non-Insulin-Dependent 		0.120 GeneticVariation GWASCAT ZRANB3 is an African-specific type 2 diabetes locus associated with beta-cell mass and insulin response. 31324766

2019
Entrez Id: 84083
Gene Symbol: ZRANB3
ZRANB3
CUI: C0011860
Disease: Diabetes Mellitus, Non-Insulin-Dependent
Diabetes Mellitus, Non-Insulin-Dependent 		0.120 GeneticVariation GWASCAT ZRANB3 is an African-specific type 2 diabetes locus associated with beta-cell mass and insulin response. 31324766

2019
Entrez Id: 3786
Gene Symbol: KCNQ3
KCNQ3
CUI: C0011860
Disease: Diabetes Mellitus, Non-Insulin-Dependent
Diabetes Mellitus, Non-Insulin-Dependent 		0.100 GeneticVariation GWASCAT ZRANB3 is an African-specific type 2 diabetes locus associated with beta-cell mass and insulin response. 31324766

2019
Entrez Id: 51384
Gene Symbol: WNT16
WNT16
CUI: C0005938
Disease: Bone Density
Bone Density 		0.100 GeneticVariation GWASCAT WNT16 influences bone mineral density, cortical bone thickness, bone strength, and osteoporotic fracture risk. 22792071

2012
Entrez Id: 7077
Gene Symbol: TIMP2
TIMP2
CUI: C0013312
Disease: Dupuytren Contracture
Dupuytren Contracture 		0.100 GeneticVariation GWASCAT Wnt signaling and Dupuytren's disease. 21732829

2011
Entrez Id: 54749
Gene Symbol: EPDR1
EPDR1
CUI: C0013312
Disease: Dupuytren Contracture
Dupuytren Contracture 		0.100 GeneticVariation GWASCAT Wnt signaling and Dupuytren's disease. 21732829

2011
Entrez Id: 7472
Gene Symbol: WNT2
WNT2
CUI: C0013312
Disease: Dupuytren Contracture
Dupuytren Contracture 		0.100 GeneticVariation GWASCAT Wnt signaling and Dupuytren's disease. 21732829

2011
Entrez Id: 100653515
Gene Symbol: CEP295NL
CEP295NL
CUI: C0013312
Disease: Dupuytren Contracture
Dupuytren Contracture 		0.100 GeneticVariation GWASCAT Wnt signaling and Dupuytren's disease. 21732829

2011
Entrez Id: 503835
Gene Symbol: DUXA
DUXA
CUI: C0013312
Disease: Dupuytren Contracture
Dupuytren Contracture 		0.100 GeneticVariation GWASCAT Wnt signaling and Dupuytren's disease. 21732829

2011
Entrez Id: 3646
Gene Symbol: EIF3E
EIF3E
CUI: C0013312
Disease: Dupuytren Contracture
Dupuytren Contracture 		0.100 GeneticVariation GWASCAT Wnt signaling and Dupuytren's disease. 21732829

2011
Entrez Id: 100505718
Gene Symbol: LINC01592
LINC01592
CUI: C0013312
Disease: Dupuytren Contracture
Dupuytren Contracture 		0.100 GeneticVariation GWASCAT Wnt signaling and Dupuytren's disease. 21732829

2011
Entrez Id: 6424
Gene Symbol: SFRP4
SFRP4
CUI: C0013312
Disease: Dupuytren Contracture
Dupuytren Contracture 		0.100 GeneticVariation GWASCAT Wnt signaling and Dupuytren's disease. 21732829

2011
Entrez Id: 79932
Gene Symbol: KIAA0319L
KIAA0319L
CUI: C0024141
Disease: Lupus Erythematosus, Systemic
Lupus Erythematosus, Systemic 		0.410 GeneticVariation GWASCAT With these, we add three (KIAA0319L, PXK and JAZF1) and one (KIAA0319L) new susceptibility loci for SSc and SLE, respectively, increasing significantly the knowledge of the genetic basis of autoimmunity. 23740937

2013
Entrez Id: 150356
Gene Symbol: CHADL
CHADL
CUI: C0029408
Disease: Degenerative polyarthritis
Degenerative polyarthritis 		0.110 GeneticVariation GWASCAT Whole-genome sequencing identifies rare genotypes in COMP and CHADL associated with high risk of hip osteoarthritis. 28319091

2017
Entrez Id: 627
Gene Symbol: BDNF
BDNF
CUI: C0005910
Disease: Body Weight
Body Weight 		0.400 GeneticVariation GWASCAT Whole-Genome Sequencing Coupled to Imputation Discovers Genetic Signals for Anthropometric Traits. 28552196

2017
Entrez Id: 79068
Gene Symbol: FTO
FTO
CUI: C0005910
Disease: Body Weight
Body Weight 		0.400 GeneticVariation GWASCAT Whole-Genome Sequencing Coupled to Imputation Discovers Genetic Signals for Anthropometric Traits. 28552196

2017
Entrez Id: 2099
Gene Symbol: ESR1
ESR1
CUI: C0005890
Disease: Body Height
Body Height 		0.100 GeneticVariation GWASCAT Whole-Genome Sequencing Coupled to Imputation Discovers Genetic Signals for Anthropometric Traits. 28552196

2017
Entrez Id: 51379
Gene Symbol: CRLF3
CRLF3
CUI: C0005890
Disease: Body Height
Body Height 		0.100 GeneticVariation GWASCAT Whole-Genome Sequencing Coupled to Imputation Discovers Genetic Signals for Anthropometric Traits. 28552196

2017
Entrez Id: 8448
Gene Symbol: DOC2A
DOC2A
CUI: C0005890
Disease: Body Height
Body Height 		0.100 GeneticVariation GWASCAT Whole-Genome Sequencing Coupled to Imputation Discovers Genetic Signals for Anthropometric Traits. 28552196

2017
Entrez Id: 64223
Gene Symbol: MLST8
MLST8
CUI: C0005890
Disease: Body Height
Body Height 		0.100 GeneticVariation GWASCAT Whole-Genome Sequencing Coupled to Imputation Discovers Genetic Signals for Anthropometric Traits. 28552196

2017
Entrez Id: 54726
Gene Symbol: OTUD4
OTUD4
CUI: C0005890
Disease: Body Height
Body Height 		0.100 GeneticVariation GWASCAT Whole-Genome Sequencing Coupled to Imputation Discovers Genetic Signals for Anthropometric Traits. 28552196

2017
Entrez Id: 25836
Gene Symbol: NIPBL
NIPBL
CUI: C0005890
Disease: Body Height
Body Height 		0.100 GeneticVariation GWASCAT Whole-Genome Sequencing Coupled to Imputation Discovers Genetic Signals for Anthropometric Traits. 28552196

2017
Entrez Id: 2768
Gene Symbol: GNA12
GNA12
CUI: C0005890
Disease: Body Height
Body Height 		0.100 GeneticVariation GWASCAT Whole-Genome Sequencing Coupled to Imputation Discovers Genetic Signals for Anthropometric Traits. 28552196

2017
Entrez Id: 83643
Gene Symbol: CCDC3
CCDC3
CUI: C0005890
Disease: Body Height
Body Height 		0.100 GeneticVariation GWASCAT Whole-Genome Sequencing Coupled to Imputation Discovers Genetic Signals for Anthropometric Traits. 28552196

2017