FLT1, fms related receptor tyrosine kinase 1, 2321

N. diseases: 424; N. variants: 33
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: rs664393
rs664393 		0.851 0.080 13 28496864 non coding transcript exon variant T/A;C snv
CUI: C0024117
Disease: Chronic Obstructive Airway Disease
Chronic Obstructive Airway Disease 		Respiratory Tract Diseases 0.010 < 0.001 1 2014 2014
dbSNP: rs664393
rs664393 		0.851 0.080 13 28496864 non coding transcript exon variant T/A;C snv
CUI: C1306460
Disease: Primary malignant neoplasm of lung
Primary malignant neoplasm of lung 		Neoplasms; Respiratory Tract Diseases 0.010 < 0.001 1 2014 2014
dbSNP: rs664393
rs664393 		0.851 0.080 13 28496864 non coding transcript exon variant T/A;C snv
CUI: C0684249
Disease: Carcinoma of lung
Carcinoma of lung 		Neoplasms; Respiratory Tract Diseases 0.010 < 0.001 1 2014 2014
dbSNP: rs664393
rs664393 		0.851 0.080 13 28496864 non coding transcript exon variant T/A;C snv
CUI: C0242379
Disease: Malignant neoplasm of lung
Malignant neoplasm of lung 		Neoplasms; Respiratory Tract Diseases 0.010 < 0.001 1 2014 2014
dbSNP: rs600640
rs600640 		13 28489832 intron variant G/A snv 0.61
CUI: C0034885
Disease: Rectal Neoplasms
Rectal Neoplasms 		Digestive System Diseases; Neoplasms 0.010 1.000 1 2014 2014
dbSNP: rs12858139
rs12858139 		1.000 0.040 13 28483931 intron variant A/C snv 0.44
CUI: C0036202
Disease: Sarcoidosis
Sarcoidosis 		Hemic and Lymphatic Diseases 0.010 1.000 1 2010 2010
dbSNP: rs74412485
rs74412485 		1.000 0.040 13 28468295 intron variant G/A snv 1.1E-03
CUI: C1956346
Disease: Coronary Artery Disease
Coronary Artery Disease 		Cardiovascular Diseases 0.010 1.000 1 2016 2016
dbSNP: rs1924981
rs1924981 		1.000 0.040 13 28448508 intron variant C/T snv 0.32
CUI: C1956346
Disease: Coronary Artery Disease
Coronary Artery Disease 		Cardiovascular Diseases 0.700 1.000 1 2017 2017
dbSNP: rs4771249
rs4771249 		13 28439277 intron variant G/A;C snv
CUI: C0009375
Disease: Colonic Neoplasms
Colonic Neoplasms 		Digestive System Diseases; Neoplasms 0.010 1.000 1 2014 2014
dbSNP: rs4771249
rs4771249 		13 28439277 intron variant G/A;C snv
CUI: C0027651
Disease: Neoplasms
Neoplasms 		Neoplasms 0.010 1.000 1 2014 2014
dbSNP: rs9513115
rs9513115 		1.000 0.040 13 28437433 intron variant C/A snv 0.77
CUI: C0242383
Disease: Age related macular degeneration
Age related macular degeneration 		Eye Diseases 0.010 1.000 1 2014 2014
dbSNP: rs7324510
rs7324510 		1.000 0.120 13 28432898 intron variant C/A;G snv
CUI: C0003873
Disease: Rheumatoid Arthritis
Rheumatoid Arthritis 		Skin and Connective Tissue Diseases; Musculoskeletal Diseases; Immune System Diseases 0.010 1.000 1 2017 2017
dbSNP: rs3794405
rs3794405 		1.000 0.080 13 28432710 intron variant C/T snv 0.77
CUI: C0279628
Disease: Adenocarcinoma Of Esophagus
Adenocarcinoma Of Esophagus 		Digestive System Diseases; Neoplasms 0.010 1.000 1 2015 2015
dbSNP: rs1432734867
rs1432734867 		1.000 0.040 13 28431232 missense variant T/C snv
CUI: C0334511
Disease: Pleural Solitary Fibrous Tumor
Pleural Solitary Fibrous Tumor 		Neoplasms 0.010 1.000 1 2018 2018
dbSNP: rs9513112
rs9513112 		1.000 0.040 13 28423565 intron variant G/A snv 0.30
CUI: C1956346
Disease: Coronary Artery Disease
Coronary Artery Disease 		Cardiovascular Diseases 0.700 1.000 1 2018 2018
dbSNP: rs9513111
rs9513111 		0.882 0.080 13 28423426 intron variant C/T snv 0.75
CUI: C0007847
Disease: Malignant tumor of cervix
Malignant tumor of cervix 		Neoplasms; Female Urogenital Diseases and Pregnancy Complications 0.010 1.000 1 2019 2019
dbSNP: rs9513111
rs9513111 		0.882 0.080 13 28423426 intron variant C/T snv 0.75
CUI: C0302592
Disease: Cervix carcinoma
Cervix carcinoma 		Neoplasms; Female Urogenital Diseases and Pregnancy Complications 0.010 1.000 1 2019 2019
dbSNP: rs9513111
rs9513111 		0.882 0.080 13 28423426 intron variant C/T snv 0.75
CUI: C4048328
Disease: cervical cancer
cervical cancer 		Neoplasms; Female Urogenital Diseases and Pregnancy Complications 0.010 1.000 1 2019 2019
dbSNP: rs9943922
rs9943922 		1.000 0.040 13 28420518 intron variant T/C snv 0.42
CUI: C0242383
Disease: Age related macular degeneration
Age related macular degeneration 		Eye Diseases 0.020 1.000 2 2016 2018
dbSNP: rs9508025
rs9508025 		0.925 0.040 13 28409926 intron variant C/G;T snv
CUI: C1956346
Disease: Coronary Artery Disease
Coronary Artery Disease 		Cardiovascular Diseases 0.020 1.000 2 2013 2016
dbSNP: rs9508025
rs9508025 		0.925 0.040 13 28409926 intron variant C/G;T snv
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease 		Cardiovascular Diseases 0.800 1.000 1 2013 2013
dbSNP: rs9319428
rs9319428 		0.925 0.080 13 28399484 intron variant G/A snv 0.30
CUI: C1956346
Disease: Coronary Artery Disease
Coronary Artery Disease 		Cardiovascular Diseases 0.800 1.000 2 2013 2018
dbSNP: rs9319428
rs9319428 		0.925 0.080 13 28399484 intron variant G/A snv 0.30
CUI: C1561643
Disease: Chronic Kidney Diseases
Chronic Kidney Diseases 		Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases 0.010 1.000 1 2015 2015
dbSNP: rs9319428
rs9319428 		0.925 0.080 13 28399484 intron variant G/A snv 0.30
CUI: C0027051
Disease: Myocardial Infarction
Myocardial Infarction 		Pathological Conditions, Signs and Symptoms; Cardiovascular Diseases 0.010 1.000 1 2015 2015
dbSNP: rs9319428
rs9319428 		0.925 0.080 13 28399484 intron variant G/A snv 0.30
CUI: C0242339
Disease: Dyslipidemias
Dyslipidemias 		Nutritional and Metabolic Diseases 0.010 1.000 1 2015 2015