Source: GWASCAT

Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs2786098
rs2786098
CRB1
CUI: C0004096
Disease: Asthma
Asthma 		0.810 GeneticVariation GWASCAT We observed replication of the association of asthma with SNP rs2786098 in the independent series of persons of European ancestry (combined P=9.3x10(-11)). 20032318

2010
dbSNP: rs1009188
rs1009188
CRB1
CUI: C1305855
Disease: Body mass index
Body mass index 		T 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: rs10754220
rs10754220
CRB1
CUI: C1305855
Disease: Body mass index
Body mass index 		G 0.700 GeneticVariation GWASCAT A Large Multiethnic Genome-Wide Association Study of Adult Body Mass Index Identifies Novel Loci. 30108127

2018
dbSNP: rs10754220
rs10754220
CRB1
CUI: C1305855
Disease: Body mass index
Body mass index 		A 0.700 GeneticVariation GWASCAT Genome-wide association study identifies 112 new loci for body mass index in the Japanese population. 28892062

2017
dbSNP: rs12042924
rs12042924
CRB1
CUI: C0871470
Disease: Systolic Pressure
Systolic Pressure 		T 0.700 GeneticVariation GWASCAT Genetic analysis of over 1 million people identifies 535 new loci associated with blood pressure traits. 30224653

2018
dbSNP: rs2759663
rs2759663
CRB1
CUI: C0149745
Disease: Oral Ulcer
Oral Ulcer 		G 0.700 GeneticVariation GWASCAT Genome wide analysis for mouth ulcers identifies associations at immune regulatory loci. 30837455

2019
dbSNP: rs2759663
rs2759663
CRB1
CUI: C1269683
Disease: Major Depressive Disorder
Major Depressive Disorder 		G 0.700 GeneticVariation GWASCAT Genome-wide association study of depression phenotypes in UK Biobank identifies variants in excitatory synaptic pathways. 29662059

2018
dbSNP: rs2786107
rs2786107
CRB1
CUI: C0523688
Disease: Hemopexin measurement
Hemopexin measurement 		G 0.700 GeneticVariation GWASCAT Connecting genetic risk to disease end points through the human blood plasma proteome. 28240269

2017
dbSNP: rs6689858
rs6689858
CRB1
CUI: C0009447
Disease: Common Variable Immunodeficiency
Common Variable Immunodeficiency 		C 0.700 GeneticVariation GWASCAT Meta-analysis of shared genetic architecture across ten pediatric autoimmune diseases. 26301688

2015
dbSNP: rs6689858
rs6689858
CRB1
CUI: C4310768
Disease: AUTOIMMUNE DISEASE, MULTISYSTEM, INFANTILE-ONSET, 2
AUTOIMMUNE DISEASE, MULTISYSTEM, INFANTILE-ONSET, 2 		C 0.700 GeneticVariation GWASCAT Meta-analysis of shared genetic architecture across ten pediatric autoimmune diseases. 26301688

2015
dbSNP: rs6689858
rs6689858
CRB1
CUI: C0920350
Disease: Autoimmune thyroiditis
Autoimmune thyroiditis 		C 0.700 GeneticVariation GWASCAT Meta-analysis of shared genetic architecture across ten pediatric autoimmune diseases. 26301688

2015
dbSNP: rs6689858
rs6689858
CRB1
CUI: C0004364
Disease: Autoimmune Diseases
Autoimmune Diseases 		C 0.700 GeneticVariation GWASCAT Meta-analysis of shared genetic architecture across ten pediatric autoimmune diseases. 26301688

2015
dbSNP: rs6689858
rs6689858
CRB1
CUI: C3150797
Disease: AUTOIMMUNE DISEASE, SUSCEPTIBILITY TO, 6
AUTOIMMUNE DISEASE, SUSCEPTIBILITY TO, 6 		C 0.700 GeneticVariation GWASCAT Meta-analysis of shared genetic architecture across ten pediatric autoimmune diseases. 26301688

2015
dbSNP: rs6689858
rs6689858
CRB1
CUI: C0011854
Disease: Diabetes Mellitus, Insulin-Dependent
Diabetes Mellitus, Insulin-Dependent 		C 0.700 GeneticVariation GWASCAT Meta-analysis of shared genetic architecture across ten pediatric autoimmune diseases. 26301688

2015
dbSNP: rs6689858
rs6689858
CRB1
CUI: C0009324
Disease: Ulcerative Colitis
Ulcerative Colitis 		C 0.700 GeneticVariation GWASCAT Meta-analysis of shared genetic architecture across ten pediatric autoimmune diseases. 26301688

2015
dbSNP: rs6689858
rs6689858
CRB1
CUI: C3495559
Disease: Juvenile arthritis
Juvenile arthritis 		C 0.700 GeneticVariation GWASCAT Meta-analysis of shared genetic architecture across ten pediatric autoimmune diseases. 26301688

2015
dbSNP: rs6689858
rs6689858
CRB1
CUI: C0010346
Disease: Crohn Disease
Crohn Disease 		C 0.700 GeneticVariation GWASCAT Meta-analysis of shared genetic architecture across ten pediatric autoimmune diseases. 26301688

2015
dbSNP: rs6689858
rs6689858
CRB1
CUI: C0007570
Disease: Celiac Disease
Celiac Disease 		C 0.700 GeneticVariation GWASCAT Meta-analysis of shared genetic architecture across ten pediatric autoimmune diseases. 26301688

2015
dbSNP: rs6689858
rs6689858
CRB1
CUI: C0024141
Disease: Lupus Erythematosus, Systemic
Lupus Erythematosus, Systemic 		C 0.700 GeneticVariation GWASCAT Meta-analysis of shared genetic architecture across ten pediatric autoimmune diseases. 26301688

2015
dbSNP: rs6689858
rs6689858
CRB1
CUI: C0033860
Disease: Psoriasis
Psoriasis 		C 0.700 GeneticVariation GWASCAT Meta-analysis of shared genetic architecture across ten pediatric autoimmune diseases. 26301688

2015
dbSNP: rs6689858
rs6689858
CRB1
CUI: C4014795
Disease: AUTOIMMUNE DISEASE, MULTISYSTEM, INFANTILE-ONSET, 1
AUTOIMMUNE DISEASE, MULTISYSTEM, INFANTILE-ONSET, 1 		C 0.700 GeneticVariation GWASCAT Meta-analysis of shared genetic architecture across ten pediatric autoimmune diseases. 26301688

2015
dbSNP: rs6689858
rs6689858
CRB1
CUI: C0038013
Disease: Ankylosing spondylitis
Ankylosing spondylitis 		C 0.700 GeneticVariation GWASCAT Meta-analysis of shared genetic architecture across ten pediatric autoimmune diseases. 26301688

2015
dbSNP: rs76169311
rs76169311
CRB1
CUI: C0202123
Disease: Luteinizing hormone measurement
Luteinizing hormone measurement 		A 0.700 GeneticVariation GWASCAT Genome-wide association of polycystic ovary syndrome implicates alterations in gonadotropin secretion in European ancestry populations. 26284813

2015
dbSNP: rs76169311
rs76169311
CRB1
CUI: C0032460
Disease: Polycystic Ovary Syndrome
Polycystic Ovary Syndrome 		A 0.700 GeneticVariation GWASCAT Genome-wide association of polycystic ovary syndrome implicates alterations in gonadotropin secretion in European ancestry populations. 26284813

2015