Source: GWASCAT ×
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs2786098
rs2786098
Entrez Id: 23418
Gene Symbol: CRB1
CRB1
CUI: C0004096
Disease:
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
Entrez Id: 23418
Gene Symbol: CRB1
CRB1
CUI: C1305855
Disease:
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: rs2759663
rs2759663
Entrez Id: 23418
Gene Symbol: CRB1
CRB1
CUI: C0149745
Disease:
Oral Ulcer 		G 0.700 GeneticVariation GWASCAT Genome wide analysis for mouth ulcers identifies associations at immune regulatory loci. 30837455 2019
dbSNP: rs10754220
rs10754220
Entrez Id: 23418
Gene Symbol: CRB1
CRB1
CUI: C1305855
Disease:
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: rs12042924
rs12042924
Entrez Id: 23418
Gene Symbol: CRB1
CRB1
CUI: C0871470
Disease:
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
Entrez Id: 23418
Gene Symbol: CRB1
CRB1
CUI: C1269683
Disease:
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: rs10754220
rs10754220
Entrez Id: 23418
Gene Symbol: CRB1
CRB1
CUI: C1305855
Disease:
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: rs2786107
rs2786107
Entrez Id: 23418
Gene Symbol: CRB1
CRB1
CUI: C0523688
Disease:
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
Entrez Id: 23418
Gene Symbol: CRB1
CRB1
CUI: C0009447
Disease:
Common Variable Immunodeficiency 		C 0.700 GeneticVariation GWASCAT Meta-analysis of shared genetic architecture across ten pediatric autoimmune diseases. 26301688 2015
dbSNP: rs6689858
rs6689858
Entrez Id: 23418
Gene Symbol: CRB1
CRB1
CUI: C4310768
Disease:
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
Entrez Id: 23418
Gene Symbol: CRB1
CRB1
CUI: C0920350
Disease:
Autoimmune thyroiditis 		C 0.700 GeneticVariation GWASCAT Meta-analysis of shared genetic architecture across ten pediatric autoimmune diseases. 26301688 2015
dbSNP: rs6689858
rs6689858
Entrez Id: 23418
Gene Symbol: CRB1
CRB1
CUI: C0004364
Disease:
Autoimmune Diseases 		C 0.700 GeneticVariation GWASCAT Meta-analysis of shared genetic architecture across ten pediatric autoimmune diseases. 26301688 2015
dbSNP: rs6689858
rs6689858
Entrez Id: 23418
Gene Symbol: CRB1
CRB1
CUI: C3150797
Disease:
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
Entrez Id: 23418
Gene Symbol: CRB1
CRB1
CUI: C0011854
Disease:
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
Entrez Id: 23418
Gene Symbol: CRB1
CRB1
CUI: C0009324
Disease:
Ulcerative Colitis 		C 0.700 GeneticVariation GWASCAT Meta-analysis of shared genetic architecture across ten pediatric autoimmune diseases. 26301688 2015
dbSNP: rs6689858
rs6689858
Entrez Id: 23418
Gene Symbol: CRB1
CRB1
CUI: C3495559
Disease:
Juvenile arthritis 		C 0.700 GeneticVariation GWASCAT Meta-analysis of shared genetic architecture across ten pediatric autoimmune diseases. 26301688 2015
dbSNP: rs6689858
rs6689858
Entrez Id: 23418
Gene Symbol: CRB1
CRB1
CUI: C0010346
Disease:
Crohn Disease 		C 0.700 GeneticVariation GWASCAT Meta-analysis of shared genetic architecture across ten pediatric autoimmune diseases. 26301688 2015
dbSNP: rs6689858
rs6689858
Entrez Id: 23418
Gene Symbol: CRB1
CRB1
CUI: C0007570
Disease:
Celiac Disease 		C 0.700 GeneticVariation GWASCAT Meta-analysis of shared genetic architecture across ten pediatric autoimmune diseases. 26301688 2015
dbSNP: rs6689858
rs6689858
Entrez Id: 23418
Gene Symbol: CRB1
CRB1
CUI: C0024141
Disease:
Lupus Erythematosus, Systemic 		C 0.700 GeneticVariation GWASCAT Meta-analysis of shared genetic architecture across ten pediatric autoimmune diseases. 26301688 2015
dbSNP: rs6689858
rs6689858
Entrez Id: 23418
Gene Symbol: CRB1
CRB1
CUI: C0033860
Disease:
Psoriasis 		C 0.700 GeneticVariation GWASCAT Meta-analysis of shared genetic architecture across ten pediatric autoimmune diseases. 26301688 2015
dbSNP: rs6689858
rs6689858
Entrez Id: 23418
Gene Symbol: CRB1
CRB1
CUI: C4014795
Disease:
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
Entrez Id: 23418
Gene Symbol: CRB1
CRB1
CUI: C0038013
Disease:
Ankylosing spondylitis 		C 0.700 GeneticVariation GWASCAT Meta-analysis of shared genetic architecture across ten pediatric autoimmune diseases. 26301688 2015
dbSNP: rs76169311
rs76169311
Entrez Id: 23418
Gene Symbol: CRB1
CRB1
CUI: C0202123
Disease:
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
Entrez Id: 23418
Gene Symbol: CRB1
CRB1
CUI: C0032460
Disease:
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