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: 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: 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: 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: C0279628
Disease: Adenocarcinoma Of Esophagus
Adenocarcinoma Of Esophagus
Digestive System Diseases; Neoplasms 0.010 1.000 1 2012 2012
dbSNP: rs7324547
rs7324547
1.000 0.080 13 28355470 intron variant A/G snv 0.64
CUI: C0279628
Disease: Adenocarcinoma Of Esophagus
Adenocarcinoma Of Esophagus
Digestive System Diseases; Neoplasms 0.010 1.000 1 2012 2012
dbSNP: rs950473882
rs950473882
13 28389975 missense variant T/C snv
CUI: C0006826
Disease: Malignant Neoplasms
Malignant Neoplasms
Neoplasms 0.010 1.000 1 2012 2012
dbSNP: rs950473882
rs950473882
13 28389975 missense variant T/C snv
CUI: C1306459
Disease: Primary malignant neoplasm
Primary malignant neoplasm
Neoplasms 0.010 1.000 1 2012 2012
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: 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: 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
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: rs7326277
rs7326277
0.851 0.080 13 28302077 3 prime UTR variant T/C snv 0.21
CUI: C0684249
Disease: Carcinoma of lung
Carcinoma of lung
Neoplasms; Respiratory Tract Diseases 0.010 1.000 1 2014 2014
dbSNP: rs7326277
rs7326277
0.851 0.080 13 28302077 3 prime UTR variant T/C snv 0.21
CUI: C0242379
Disease: Malignant neoplasm of lung
Malignant neoplasm of lung
Neoplasms; Respiratory Tract Diseases 0.010 1.000 1 2014 2014
dbSNP: rs7326277
rs7326277
0.851 0.080 13 28302077 3 prime UTR variant T/C snv 0.21
CUI: C0024117
Disease: Chronic Obstructive Airway Disease
Chronic Obstructive Airway Disease
Respiratory Tract Diseases 0.010 1.000 1 2014 2014
dbSNP: rs7326277
rs7326277
0.851 0.080 13 28302077 3 prime UTR variant T/C snv 0.21
CUI: C1306460
Disease: Primary malignant neoplasm of lung
Primary malignant neoplasm of lung
Neoplasms; Respiratory Tract Diseases 0.010 1.000 1 2014 2014
dbSNP: rs7983774
rs7983774
13 28390188 intron variant G/A;T snv
CUI: C0034885
Disease: Rectal Neoplasms
Rectal Neoplasms
Digestive System Diseases; Neoplasms 0.010 1.000 1 2014 2014
dbSNP: rs7987649
rs7987649
0.925 0.080 13 28320278 intron variant A/G snv 0.35
CUI: C0699790
Disease: Colon Carcinoma
Colon Carcinoma
Digestive System Diseases; Neoplasms 0.010 1.000 1 2014 2014
dbSNP: rs7987649
rs7987649
0.925 0.080 13 28320278 intron variant A/G snv 0.35
CUI: C0007102
Disease: Malignant tumor of colon
Malignant tumor of colon
Digestive System Diseases; Neoplasms 0.010 1.000 1 2014 2014
dbSNP: rs7987649
rs7987649
0.925 0.080 13 28320278 intron variant A/G snv 0.35
CUI: C0009375
Disease: Colonic Neoplasms
Colonic Neoplasms
Digestive System Diseases; Neoplasms 0.010 1.000 1 2014 2014