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: 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: 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: 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: rs9508017
rs9508017 		13 28360227 intron variant C/T snv 0.23
CUI: C0005612
Disease: Birth Weight
Birth Weight 		Pathological Conditions, Signs and Symptoms 0.700 1.000 1 2019 2019
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: 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
dbSNP: rs9582036
rs9582036 		0.776 0.280 13 28311271 intron variant C/A snv 0.59
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: rs9582036
rs9582036 		0.776 0.280 13 28311271 intron variant C/A snv 0.59
CUI: C0278678
Disease: Metastatic Renal Cell Cancer
Metastatic Renal Cell Cancer 		0.030 1.000 3 2014 2017
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: 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: 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: 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: rs17619601
rs17619601 		1.000 0.080 13 28326373 intron variant C/T snv 5.0E-02
CUI: C0279628
Disease: Adenocarcinoma Of Esophagus
Adenocarcinoma Of Esophagus 		Digestive System Diseases; Neoplasms 0.010 1.000 1 2012 2012
dbSNP: rs17625898
rs17625898 		1.000 0.080 13 28358693 intron variant T/A;G snv
CUI: C0279628
Disease: Adenocarcinoma Of Esophagus
Adenocarcinoma Of Esophagus 		Digestive System Diseases; Neoplasms 0.010 1.000 1 2012 2012
dbSNP: rs2296188
rs2296188 		0.925 0.200 13 28319347 intron variant T/C snv 0.70
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: rs2296188
rs2296188 		0.925 0.200 13 28319347 intron variant T/C snv 0.70
CUI: C0279628
Disease: Adenocarcinoma Of Esophagus
Adenocarcinoma Of Esophagus 		Digestive System Diseases; Neoplasms 0.010 1.000 1 2012 2012
dbSNP: rs2296189
rs2296189 		13 28319505 synonymous variant A/C;G snv 8.0E-06; 0.21
CUI: C0034885
Disease: Rectal Neoplasms
Rectal Neoplasms 		Digestive System Diseases; Neoplasms 0.010 1.000 1 2014 2014
dbSNP: rs2296283
rs2296283 		1.000 0.040 13 28389565 3 prime UTR variant G/A snv 0.42
CUI: C0036202
Disease: Sarcoidosis
Sarcoidosis 		Hemic and Lymphatic Diseases 0.010 1.000 1 2010 2010
dbSNP: rs377395740
rs377395740 		1.000 0.040 13 28389988 missense variant G/A;C;T snv 4.4E-05; 4.0E-06; 4.0E-06
CUI: C0334511
Disease: Pleural Solitary Fibrous Tumor
Pleural Solitary Fibrous Tumor 		Neoplasms 0.010 1.000 1 2018 2018
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: 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: 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: 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