CCL20, C-C motif chemokine ligand 20, 6364

N. diseases: 242; N. variants: 3
Source: ALL
Variant DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Disease Disease Class Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs10175070
rs10175070 		1.000 0.080 2 227805859 5 prime UTR variant G/A;C snv
CUI: C0264408
Disease: Childhood asthma
Childhood asthma 		Respiratory Tract Diseases; Immune System Diseases 0.700 1.000 1 2019 2019
dbSNP: rs1811711
rs1811711 		1.000 0.040 2 227805760 5 prime UTR variant C/A;G snv
CUI: C0009324
Disease: Ulcerative Colitis
Ulcerative Colitis 		Digestive System Diseases 0.700 1.000 1 2017 2017
dbSNP: rs1811711
rs1811711 		1.000 0.040 2 227805760 5 prime UTR variant C/A;G snv
CUI: C0021390
Disease: Inflammatory Bowel Diseases
Inflammatory Bowel Diseases 		Digestive System Diseases 0.700 1.000 1 2017 2017
dbSNP: rs6749704
rs6749704 		0.827 0.240 2 227813126 intron variant T/C snv 0.24
CUI: C0026769
Disease: Multiple Sclerosis
Multiple Sclerosis 		Immune System Diseases; Nervous System Diseases 0.020 1.000 2 2014 2019
dbSNP: rs6749704
rs6749704 		0.827 0.240 2 227813126 intron variant T/C snv 0.24
CUI: C0011860
Disease: Diabetes Mellitus, Non-Insulin-Dependent
Diabetes Mellitus, Non-Insulin-Dependent 		Nutritional and Metabolic Diseases; Endocrine System Diseases 0.010 1.000 1 2019 2019
dbSNP: rs6749704
rs6749704 		0.827 0.240 2 227813126 intron variant T/C snv 0.24
CUI: C0151744
Disease: Myocardial Ischemia
Myocardial Ischemia 		Cardiovascular Diseases 0.010 < 0.001 1 2016 2016
dbSNP: rs6749704
rs6749704 		0.827 0.240 2 227813126 intron variant T/C snv 0.24
CUI: C0026269
Disease: Mitral Valve Stenosis
Mitral Valve Stenosis 		Cardiovascular Diseases 0.010 1.000 1 2019 2019
dbSNP: rs6749704
rs6749704 		0.827 0.240 2 227813126 intron variant T/C snv 0.24
CUI: C0028754
Disease: Obesity
Obesity 		Pathological Conditions, Signs and Symptoms; Nutritional and Metabolic Diseases 0.010 1.000 1 2019 2019