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: rs7987649
rs7987649 		0.925 0.080 13 28320278 intron variant A/G snv 0.35
CUI: C0027651
Disease: Neoplasms
Neoplasms 		Neoplasms 0.010 1.000 1 2014 2014
dbSNP: rs7993418
rs7993418 		0.925 0.120 13 28308924 synonymous variant G/A snv 0.80 0.67
CUI: C0346647
Disease: Malignant neoplasm of pancreas
Malignant neoplasm of pancreas 		Digestive System Diseases; Neoplasms; Endocrine System Diseases 0.010 1.000 1 2014 2014
dbSNP: rs7993418
rs7993418 		0.925 0.120 13 28308924 synonymous variant G/A snv 0.80 0.67
CUI: C0235974
Disease: Pancreatic carcinoma
Pancreatic carcinoma 		Digestive System Diseases; Neoplasms; Endocrine System Diseases 0.010 1.000 1 2014 2014
dbSNP: rs9513070
rs9513070 		0.851 0.080 13 28305702 intron variant G/A snv 0.54
CUI: C0009402
Disease: Colorectal Carcinoma
Colorectal Carcinoma 		Digestive System Diseases; 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: rs9554314
rs9554314 		0.851 0.080 13 28301652 3 prime UTR variant 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: rs9554314
rs9554314 		0.851 0.080 13 28301652 3 prime UTR variant 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: rs9554314
rs9554314 		0.851 0.080 13 28301652 3 prime UTR variant A/C snv
CUI: C0684249
Disease: Carcinoma of lung
Carcinoma of lung 		Neoplasms; Respiratory Tract Diseases 0.010 < 0.001 1 2014 2014
dbSNP: rs9554314
rs9554314 		0.851 0.080 13 28301652 3 prime UTR variant 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: rs9582036
rs9582036 		0.776 0.280 13 28311271 intron variant C/A snv 0.59
CUI: C0235974
Disease: Pancreatic carcinoma
Pancreatic carcinoma 		Digestive System Diseases; Neoplasms; Endocrine System Diseases 0.010 1.000 1 2014 2014
dbSNP: rs9582036
rs9582036 		0.776 0.280 13 28311271 intron variant C/A snv 0.59
CUI: C0346647
Disease: Malignant neoplasm of pancreas
Malignant neoplasm of pancreas 		Digestive System Diseases; Neoplasms; Endocrine System Diseases 0.010 1.000 1 2014 2014
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: 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
dbSNP: rs9582036
rs9582036 		0.776 0.280 13 28311271 intron variant C/A snv 0.59
CUI: C0007131
Disease: Non-Small Cell Lung Carcinoma
Non-Small Cell Lung Carcinoma 		Neoplasms; Respiratory Tract Diseases 0.010 1.000 1 2015 2015
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: 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: rs9554320
rs9554320 		0.882 0.160 13 28312790 intron variant A/C;G snv
CUI: C0242383
Disease: Age related macular degeneration
Age related macular degeneration 		Eye Diseases 0.010 1.000 1 2016 2016
dbSNP: rs9554322
rs9554322 		1.000 0.040 13 28339694 intron variant G/C;T snv
CUI: C0242383
Disease: Age related macular degeneration
Age related macular degeneration 		Eye Diseases 0.010 1.000 1 2016 2016
dbSNP: rs9582036
rs9582036 		0.776 0.280 13 28311271 intron variant C/A snv 0.59
CUI: C0242383
Disease: Age related macular degeneration
Age related macular degeneration 		Eye Diseases 0.010 1.000 1 2016 2016
dbSNP: rs9582036
rs9582036 		0.776 0.280 13 28311271 intron variant C/A snv 0.59
CUI: C0279702
Disease: Conventional (Clear Cell) Renal Cell Carcinoma
Conventional (Clear Cell) Renal Cell Carcinoma 		Neoplasms; Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases 0.010 1.000 1 2016 2016
dbSNP: rs9582036
rs9582036 		0.776 0.280 13 28311271 intron variant C/A snv 0.59
CUI: C0014175
Disease: Endometriosis
Endometriosis 		Female Urogenital Diseases and Pregnancy Complications 0.010 1.000 1 2016 2016
dbSNP: rs9554320
rs9554320 		0.882 0.160 13 28312790 intron variant A/C;G snv
CUI: C4721698
Disease: Metastatic Renal Cell Carcinoma
Metastatic Renal Cell Carcinoma 		Neoplasms; Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases 0.030 1.000 3 2014 2017
dbSNP: rs9554320
rs9554320 		0.882 0.160 13 28312790 intron variant A/C;G snv
CUI: C0278678
Disease: Metastatic Renal Cell Cancer
Metastatic Renal Cell Cancer 		0.030 1.000 3 2014 2017