FGFR1OP, FGFR1 oncogene partner, 11116

N. diseases: 40; N. variants: 9
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs2301436
rs2301436
Entrez Id: 11116
Gene Symbol: FGFR1OP
FGFR1OP
CUI: C0010346
Disease:
Crohn Disease 		0.810 GeneticVariation GWASCAT Analysis of five chronic inflammatory diseases identifies 27 new associations and highlights disease-specific patterns at shared loci. 26974007 2016
dbSNP: rs2301436
rs2301436
Entrez Id: 11116
Gene Symbol: FGFR1OP
FGFR1OP
CUI: C0010346
Disease:
Crohn Disease 		0.810 GeneticVariation BEFREE Here, we studied the susceptibility nature of three components of IL23 signalling and Th17 cell differentiation: JAK2 rs10758669, STAT3 rs744166 and CCR6 rs2301436 initially associated with CD in Hungarian CD and UC patients. 22269120 2012
dbSNP: rs2301436
rs2301436
Entrez Id: 11116
Gene Symbol: FGFR1OP
FGFR1OP
CUI: C0010346
Disease:
Crohn Disease 		0.810 GeneticVariation GWASCAT Fucosyltransferase 2 (FUT2) non-secretor status is associated with Crohn's disease. 20570966 2010
dbSNP: rs2301436
rs2301436
Entrez Id: 11116
Gene Symbol: FGFR1OP
FGFR1OP
CUI: C0010346
Disease:
Crohn Disease 		0.810 GeneticVariation GWASDB Fucosyltransferase 2 (FUT2) non-secretor status is associated with Crohn's disease. 20570966 2010
dbSNP: rs2301436
rs2301436
Entrez Id: 11116
Gene Symbol: FGFR1OP
FGFR1OP
CUI: C0010346
Disease:
Crohn Disease 		T 0.810 GeneticVariation GWASDB Genome-wide association defines more than 30 distinct susceptibility loci for Crohn's disease. 18587394 2008
dbSNP: rs2301436
rs2301436
Entrez Id: 11116
Gene Symbol: FGFR1OP
FGFR1OP
CUI: C0010346
Disease:
Crohn Disease 		T 0.810 GeneticVariation GWASCAT Genome-wide association defines more than 30 distinct susceptibility loci for Crohn's disease. 18587394 2008
dbSNP: rs2301436
rs2301436
Entrez Id: 11116
Gene Symbol: FGFR1OP
FGFR1OP
CUI: C0009324
Disease:
Ulcerative Colitis 		0.710 GeneticVariation GWASCAT Analysis of five chronic inflammatory diseases identifies 27 new associations and highlights disease-specific patterns at shared loci. 26974007 2016
dbSNP: rs2301436
rs2301436
Entrez Id: 11116
Gene Symbol: FGFR1OP
FGFR1OP
CUI: C0009324
Disease:
Ulcerative Colitis 		0.710 GeneticVariation BEFREE Here, we studied the susceptibility nature of three components of IL23 signalling and Th17 cell differentiation: JAK2 rs10758669, STAT3 rs744166 and CCR6 rs2301436 initially associated with CD in Hungarian CD and UC patients. 22269120 2012
dbSNP: rs2301436
rs2301436
Entrez Id: 11116
Gene Symbol: FGFR1OP
FGFR1OP
CUI: C0033860
Disease:
Psoriasis 		0.700 GeneticVariation GWASCAT Analysis of five chronic inflammatory diseases identifies 27 new associations and highlights disease-specific patterns at shared loci. 26974007 2016
dbSNP: rs2301436
rs2301436
Entrez Id: 11116
Gene Symbol: FGFR1OP
FGFR1OP
CUI: C0038013
Disease:
Ankylosing spondylitis 		0.700 GeneticVariation GWASCAT Analysis of five chronic inflammatory diseases identifies 27 new associations and highlights disease-specific patterns at shared loci. 26974007 2016
dbSNP: rs2301436
rs2301436
Entrez Id: 11116
Gene Symbol: FGFR1OP
FGFR1OP
CUI: C0008313
Disease:
Cholangitis, Sclerosing 		0.700 GeneticVariation GWASCAT Analysis of five chronic inflammatory diseases identifies 27 new associations and highlights disease-specific patterns at shared loci. 26974007 2016
dbSNP: rs368397331
rs368397331
Entrez Id: 11116
Gene Symbol: FGFR1OP
FGFR1OP
CUI: C0018213
Disease:
Graves Disease 		0.700 GeneticVariation GWASDB Seven newly identified loci for autoimmune thyroid disease. 22922229 2012
dbSNP: rs6902119
rs6902119
Entrez Id: 11116
Gene Symbol: FGFR1OP
FGFR1OP
CUI: C0042900
Disease:
Vitiligo 		0.700 GeneticVariation GWASDB Genome-wide association analyses identify 13 new susceptibility loci for generalized vitiligo. 22561518 2012
dbSNP: rs12526548
rs12526548
Entrez Id: 11116
Gene Symbol: FGFR1OP
FGFR1OP
CUI: C0018213
Disease:
Graves Disease 		0.700 GeneticVariation GWASDB A genome-wide association study identifies two new risk loci for Graves' disease. 21841780 2011
dbSNP: rs204295
rs204295
Entrez Id: 11116
Gene Symbol: FGFR1OP
FGFR1OP
CUI: C0018213
Disease:
Graves Disease 		0.700 GeneticVariation GWASDB A genome-wide association study identifies two new risk loci for Graves' disease. 21841780 2011
dbSNP: rs2301436
rs2301436
Entrez Id: 11116
Gene Symbol: FGFR1OP
FGFR1OP
CUI: C0026769
Disease:
Multiple Sclerosis 		0.700 GeneticVariation GWASDB Genome-wide meta-analysis identifies novel multiple sclerosis susceptibility loci. 22190364 2011
dbSNP: rs2301436
rs2301436
Entrez Id: 11116
Gene Symbol: FGFR1OP
FGFR1OP
CUI: C0004096
Disease:
Asthma 		0.700 GeneticVariation GWASDB Association between ORMDL3, IL1RL1 and a deletion on chromosome 17q21 with asthma risk in Australia. 21150878 2011
dbSNP: rs2301436
rs2301436
Entrez Id: 11116
Gene Symbol: FGFR1OP
FGFR1OP
CUI: C0018213
Disease:
Graves Disease 		0.700 GeneticVariation GWASDB A genome-wide association study identifies two new risk loci for Graves' disease. 21841780 2011
dbSNP: rs6902119
rs6902119
Entrez Id: 11116
Gene Symbol: FGFR1OP
FGFR1OP
CUI: C0042900
Disease:
Vitiligo 		0.700 GeneticVariation GWASDB Genome-wide association study for vitiligo identifies susceptibility loci at 6q27 and the MHC. 20526339 2010
dbSNP: rs7749278
rs7749278
Entrez Id: 11116
Gene Symbol: FGFR1OP
FGFR1OP
CUI: C0010346
Disease:
Crohn Disease 		0.700 GeneticVariation GWASDB Genome-wide association defines more than 30 distinct susceptibility loci for Crohn's disease. 18587394 2008
dbSNP: rs12212247
rs12212247
Entrez Id: 11116
Gene Symbol: FGFR1OP
FGFR1OP
CUI: C0242379
Disease:
Malignant neoplasm of lung 		0.010 GeneticVariation BEFREE Another significant tagSNP rs12212247 T>C (P combined = 9.589 × 10(-6)) was associated with a decreased risk of lung cancer (OR = 0.93, 95% CI = 0.90-0.96). 26905588 2016
dbSNP: rs12212247
rs12212247
Entrez Id: 11116
Gene Symbol: FGFR1OP
FGFR1OP
CUI: C1306460
Disease:
Primary malignant neoplasm of lung 		0.010 GeneticVariation BEFREE Another significant tagSNP rs12212247 T>C (P combined = 9.589 × 10(-6)) was associated with a decreased risk of lung cancer (OR = 0.93, 95% CI = 0.90-0.96). 26905588 2016
dbSNP: rs12212247
rs12212247
Entrez Id: 11116
Gene Symbol: FGFR1OP
FGFR1OP
CUI: C0684249
Disease:
Carcinoma of lung 		0.010 GeneticVariation BEFREE Another significant tagSNP rs12212247 T>C (P combined = 9.589 × 10(-6)) was associated with a decreased risk of lung cancer (OR = 0.93, 95% CI = 0.90-0.96). 26905588 2016
dbSNP: rs151606
rs151606
Entrez Id: 11116
Gene Symbol: FGFR1OP
FGFR1OP
CUI: C0684249
Disease:
Carcinoma of lung 		0.010 GeneticVariation BEFREE The rs151606 T>G was associated with an increased risk of lung cancer [odds ratio (OR) = 1.10, 95% confidence interval (95% CI) = 1.05-1.14]. 26905588 2016
dbSNP: rs151606
rs151606
Entrez Id: 11116
Gene Symbol: FGFR1OP
FGFR1OP
CUI: C1306460
Disease:
Primary malignant neoplasm of lung 		0.010 GeneticVariation BEFREE The rs151606 T>G was associated with an increased risk of lung cancer [odds ratio (OR) = 1.10, 95% confidence interval (95% CI) = 1.05-1.14]. 26905588 2016