DLEU1, deleted in lymphocytic leukemia 1, 10301

N. diseases: 109; N. variants: 65
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs2762051
rs2762051
Entrez Id: 10301
Gene Symbol: DLEU1
DLEU1
CUI: C0007570
Disease:
Celiac Disease 		0.810 GeneticVariation BEFREE These four variants are implicated in complex phenotypes such as ulcerative colitis and AIDS progression disease (rs10491434), Celiac disease (rs2762051), Crohn's disease, IgA nephropathy and early-onset inflammatory bowel disease (rs713875) and height (rs6569648). 24911414 2014
dbSNP: rs2762051
rs2762051
Entrez Id: 10301
Gene Symbol: DLEU1
DLEU1
CUI: C0007570
Disease:
Celiac Disease 		A 0.810 GeneticVariation GWASDB Multiple common variants for celiac disease influencing immune gene expression. 20190752 2010
dbSNP: rs2762051
rs2762051
Entrez Id: 10301
Gene Symbol: DLEU1
DLEU1
CUI: C0007570
Disease:
Celiac Disease 		A 0.810 GeneticVariation GWASCAT Multiple common variants for celiac disease influencing immune gene expression. 20190752 2010
dbSNP: rs806321
rs806321
Entrez Id: 10301
Gene Symbol: DLEU1
DLEU1
CUI: C0026769
Disease:
Multiple Sclerosis 		0.800 GeneticVariation GWASCAT Genetic overlap between autoimmune diseases and non-Hodgkin lymphoma subtypes. 31407831 2019
dbSNP: rs806321
rs806321
Entrez Id: 10301
Gene Symbol: DLEU1
DLEU1
CUI: C0026769
Disease:
Multiple Sclerosis 		A 0.800 GeneticVariation GWASDB Genetic risk and a primary role for cell-mediated immune mechanisms in multiple sclerosis. 21833088 2011
dbSNP: rs806321
rs806321
Entrez Id: 10301
Gene Symbol: DLEU1
DLEU1
CUI: C0026769
Disease:
Multiple Sclerosis 		A 0.800 GeneticVariation GWASCAT Genetic risk and a primary role for cell-mediated immune mechanisms in multiple sclerosis. 21833088 2011
dbSNP: rs9596270
rs9596270
Entrez Id: 10301
Gene Symbol: DLEU1
DLEU1
CUI: C0026769
Disease:
Multiple Sclerosis 		T 0.800 GeneticVariation GWASCAT Genome-wide meta-analysis identifies novel multiple sclerosis susceptibility loci. 22190364 2011
dbSNP: rs9596270
rs9596270
Entrez Id: 10301
Gene Symbol: DLEU1
DLEU1
CUI: C0026769
Disease:
Multiple Sclerosis 		T 0.800 GeneticVariation GWASDB Genome-wide meta-analysis identifies novel multiple sclerosis susceptibility loci. 22190364 2011
dbSNP: rs1149833
rs1149833
Entrez Id: 10301
Gene Symbol: DLEU1
DLEU1
CUI: C0339471
Disease:
Maculopathy with diabetes mellitus 		0.700 GeneticVariation GWASCAT A genome-wide association study implicates that the TTC39C gene is associated with diabetic maculopathy with decreased visual acuity. 31264924 2019
dbSNP: rs1149833
rs1149833
Entrez Id: 10301
Gene Symbol: DLEU1
DLEU1
CUI: C0011860
Disease:
Diabetes Mellitus, Non-Insulin-Dependent 		0.700 GeneticVariation GWASCAT A genome-wide association study implicates that the TTC39C gene is associated with diabetic maculopathy with decreased visual acuity. 31264924 2019
dbSNP: rs117496431
rs117496431
Entrez Id: 10301;220107
Gene Symbol: DLEU1;DLEU7
DLEU1;DLEU7
CUI: C0205682
Disease:
Waist-Hip Ratio 		0.700 GeneticVariation GWASCAT Leveraging Polygenic Functional Enrichment to Improve GWAS Power. 30595370 2019
dbSNP: rs123378
rs123378
Entrez Id: 10301
Gene Symbol: DLEU1
DLEU1
CUI: C0011860
Disease:
Diabetes Mellitus, Non-Insulin-Dependent 		G 0.700 GeneticVariation GWASCAT Identification of 28 new susceptibility loci for type 2 diabetes in the Japanese population. 30718926 2019
dbSNP: rs1239704
rs1239704
Entrez Id: 10301;220107
Gene Symbol: DLEU1;DLEU7
DLEU1;DLEU7
CUI: C0005890
Disease:
Body Height 		0.700 GeneticVariation GWASCAT Characterizing rare and low-frequency height-associated variants in the Japanese population. 31562340 2019
dbSNP: rs1239948
rs1239948
Entrez Id: 10301;220107
Gene Symbol: DLEU1;DLEU7
DLEU1;DLEU7
CUI: C0871470
Disease:
Systolic Pressure 		0.700 GeneticVariation GWASCAT Leveraging Polygenic Functional Enrichment to Improve GWAS Power. 30595370 2019
dbSNP: rs1239948
rs1239948
Entrez Id: 10301;220107
Gene Symbol: DLEU1;DLEU7
DLEU1;DLEU7
CUI: C0007222
Disease:
Cardiovascular Diseases 		0.700 GeneticVariation GWASCAT Leveraging Polygenic Functional Enrichment to Improve GWAS Power. 30595370 2019
dbSNP: rs1262720
rs1262720
Entrez Id: 10301;220107
Gene Symbol: DLEU1;DLEU7
DLEU1;DLEU7
CUI: C0205682
Disease:
Waist-Hip Ratio 		0.700 GeneticVariation GWASCAT Leveraging Polygenic Functional Enrichment to Improve GWAS Power. 30595370 2019
dbSNP: rs143794540
rs143794540
Entrez Id: 10301
Gene Symbol: DLEU1
DLEU1
CUI: C0005890
Disease:
Body Height 		0.700 GeneticVariation GWASCAT Leveraging Polygenic Functional Enrichment to Improve GWAS Power. 30595370 2019
dbSNP: rs201798
rs201798
Entrez Id: 10301
Gene Symbol: DLEU1
DLEU1
CUI: C0200638
Disease:
Eosinophil count procedure 		0.700 GeneticVariation GWASCAT Leveraging Polygenic Functional Enrichment to Improve GWAS Power. 30595370 2019
dbSNP: rs2066590
rs2066590
Entrez Id: 8847;10301
Gene Symbol: DLEU2;DLEU1
DLEU2;DLEU1
CUI: C0200638
Disease:
Eosinophil count procedure 		0.700 GeneticVariation GWASCAT Leveraging Polygenic Functional Enrichment to Improve GWAS Power. 30595370 2019
dbSNP: rs2762060
rs2762060
Entrez Id: 10301
Gene Symbol: DLEU1
DLEU1
CUI: C0023508
Disease:
White Blood Cell Count procedure 		0.700 GeneticVariation GWASCAT Leveraging Polygenic Functional Enrichment to Improve GWAS Power. 30595370 2019
dbSNP: rs2812208
rs2812208
Entrez Id: 10301
Gene Symbol: DLEU1
DLEU1
CUI: C0016529
Disease:
Forced expiratory volume function 		C 0.700 GeneticVariation GWASCAT New genetic signals for lung function highlight pathways and chronic obstructive pulmonary disease associations across multiple ancestries. 30804560 2019
dbSNP: rs2812208
rs2812208
Entrez Id: 10301
Gene Symbol: DLEU1
DLEU1
CUI: C0424678
Disease:
Lean body mass 		0.700 GeneticVariation GWASCAT Genomics of body fat percentage may contribute to sex bias in anorexia nervosa. 30593698 2019
dbSNP: rs2812208
rs2812208
Entrez Id: 10301
Gene Symbol: DLEU1
DLEU1
CUI: C0042834
Disease:
Vital capacity 		0.700 GeneticVariation GWASCAT Leveraging Polygenic Functional Enrichment to Improve GWAS Power. 30595370 2019
dbSNP: rs2812208
rs2812208
Entrez Id: 10301
Gene Symbol: DLEU1
DLEU1
CUI: C0042834
Disease:
Vital capacity 		C 0.700 GeneticVariation GWASCAT New genetic signals for lung function highlight pathways and chronic obstructive pulmonary disease associations across multiple ancestries. 30804560 2019
dbSNP: rs3116590
rs3116590
Entrez Id: 10301
Gene Symbol: DLEU1
DLEU1
CUI: C0013595
Disease:
Eczema 		0.700 GeneticVariation GWASCAT Leveraging Polygenic Functional Enrichment to Improve GWAS Power. 30595370 2019