HGF, hepatocyte growth factor, 3082

N. diseases: 671; N. variants: 22
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: rs5745687
rs5745687 		1.000 0.040 7 81729735 missense variant C/T snv 4.6E-02 4.3E-02
CUI: C3266262
Disease: Multiple Chronic Conditions
Multiple Chronic Conditions 		Pathological Conditions, Signs and Symptoms 0.010 1.000 1 2015 2015
dbSNP: rs5745718
rs5745718 		0.882 0.040 7 81718232 intron variant T/G snv 0.82
CUI: C0017605
Disease: Angle Closure Glaucoma
Angle Closure Glaucoma 		Eye Diseases 0.010 1.000 1 2013 2013
dbSNP: rs5745718
rs5745718 		0.882 0.040 7 81718232 intron variant T/G snv 0.82
CUI: C0017606
Disease: Primary angle-closure glaucoma
Primary angle-closure glaucoma 		Eye Diseases 0.010 1.000 1 2013 2013
dbSNP: rs5745718
rs5745718 		0.882 0.040 7 81718232 intron variant T/G snv 0.82
CUI: C0020490
Disease: Hyperopia
Hyperopia 		Eye Diseases 0.010 1.000 1 2010 2010
dbSNP: rs5745752
rs5745752 		0.925 0.080 7 81706144 intron variant C/T snv 0.25
CUI: C0006142
Disease: Malignant neoplasm of breast
Malignant neoplasm of breast 		Neoplasms; Skin and Connective Tissue Diseases 0.010 1.000 1 2014 2014
dbSNP: rs5745752
rs5745752 		0.925 0.080 7 81706144 intron variant C/T snv 0.25
CUI: C0678222
Disease: Breast Carcinoma
Breast Carcinoma 		Neoplasms; Skin and Connective Tissue Diseases 0.010 1.000 1 2014 2014
dbSNP: rs751819844
rs751819844 		1.000 0.040 7 81705724 missense variant G/A snv 6.4E-05 2.8E-05
CUI: C0036439
Disease: Scoliosis, unspecified
Scoliosis, unspecified 		Musculoskeletal Diseases 0.010 1.000 1 2019 2019
dbSNP: rs757832
rs757832 		1.000 0.080 7 81733271 intron variant A/G;T snv
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 2015 2015
dbSNP: rs762140462
rs762140462 		1.000 0.120 7 81752245 missense variant T/C snv 4.0E-06
CUI: C0267663
Disease: Congenital secretory diarrhea, sodium type (disorder)
Congenital secretory diarrhea, sodium type (disorder) 		Pathological Conditions, Signs and Symptoms; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases 0.010 1.000 1 2014 2014
dbSNP: rs9642131
rs9642131 		1.000 0.040 7 81740948 intron variant G/T snv 0.78
CUI: C4315867
Disease: Moderate myopia
Moderate myopia 		Eye Diseases 0.010 1.000 1 2010 2010