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: C4522089
Disease: Hepatocyte Growth Factor Measurement
Hepatocyte Growth Factor Measurement 		0.700 1.000 2 2015 2017
dbSNP: rs5745642
rs5745642 		7 81756276 3 prime UTR variant G/C snv 1.6E-02
CUI: C0392885
Disease: High density lipoprotein measurement
High density lipoprotein measurement 		0.700 1.000 1 2012 2012
dbSNP: rs5745642
rs5745642 		7 81756276 3 prime UTR variant G/C snv 1.6E-02
CUI: C0428472
Disease: Serum HDL cholesterol measurement
Serum HDL cholesterol measurement 		0.700 1.000 1 2012 2012
dbSNP: rs5745695
rs5745695 		7 81728759 intron variant G/A;T snv
CUI: C2985280
Disease: Blood Protein Measurement
Blood Protein Measurement 		0.700 1.000 1 2018 2018
dbSNP: rs5745709
rs5745709 		0.925 0.120 7 81720096 intron variant T/C snv 0.85
CUI: C0003868
Disease: Arthritis, Gouty
Arthritis, Gouty 		Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Musculoskeletal Diseases 0.700 1.000 1 2012 2012
dbSNP: rs5745709
rs5745709 		0.925 0.120 7 81720096 intron variant T/C snv 0.85
CUI: C0018099
Disease: Gout
Gout 		Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Musculoskeletal Diseases 0.700 1.000 1 2012 2012
dbSNP: rs984534
rs984534 		7 81753374 intron variant C/T snv 0.83
CUI: C2985280
Disease: Blood Protein Measurement
Blood Protein Measurement 		0.700 1.000 1 2018 2018
dbSNP: rs137853235
rs137853235 		1.000 0.120 7 81752250 splice region variant C/T snv 4.0E-06
CUI: C1842342
Disease: DEAFNESS, AUTOSOMAL RECESSIVE 39 (disorder)
DEAFNESS, AUTOSOMAL RECESSIVE 39 (disorder) 		Pathological Conditions, Signs and Symptoms; Nervous System Diseases; Otorhinolaryngologic Diseases 0.700 0
dbSNP: rs12536657
rs12536657 		0.925 0.040 7 81720892 intron variant A/G snv 0.84 0.85
CUI: C0020490
Disease: Hyperopia
Hyperopia 		Eye Diseases 0.020 1.000 2 2010 2019
dbSNP: rs17427817
rs17427817 		0.925 0.040 7 81735119 intron variant C/A;G;T snv
CUI: C0017605
Disease: Angle Closure Glaucoma
Angle Closure Glaucoma 		Eye Diseases 0.020 1.000 2 2013 2018
dbSNP: rs17427817
rs17427817 		0.925 0.040 7 81735119 intron variant C/A;G;T snv
CUI: C0017606
Disease: Primary angle-closure glaucoma
Primary angle-closure glaucoma 		Eye Diseases 0.020 1.000 2 2013 2018
dbSNP: rs10272030
rs10272030 		1.000 0.040 7 81720907 intron variant G/A snv 0.85
CUI: C4315867
Disease: Moderate myopia
Moderate myopia 		Eye Diseases 0.010 1.000 1 2010 2010
dbSNP: rs12536657
rs12536657 		0.925 0.040 7 81720892 intron variant A/G snv 0.84 0.85
CUI: C4315867
Disease: Moderate myopia
Moderate myopia 		Eye Diseases 0.010 1.000 1 2010 2010
dbSNP: rs12540393
rs12540393 		0.925 0.040 7 81734871 intron variant C/T snv 0.77
CUI: C0017605
Disease: Angle Closure Glaucoma
Angle Closure Glaucoma 		Eye Diseases 0.010 1.000 1 2018 2018
dbSNP: rs12540393
rs12540393 		0.925 0.040 7 81734871 intron variant C/T snv 0.77
CUI: C0017606
Disease: Primary angle-closure glaucoma
Primary angle-closure glaucoma 		Eye Diseases 0.010 1.000 1 2018 2018
dbSNP: rs1453208391
rs1453208391 		7 81707297 missense variant G/A snv 4.0E-06
CUI: C1269955
Disease: Tumor Cell Invasion
Tumor Cell Invasion 		0.010 1.000 1 2017 2017
dbSNP: rs1743
rs1743 		1.000 0.040 7 81699165 3 prime UTR variant A/G;T snv
CUI: C4315867
Disease: Moderate myopia
Moderate myopia 		Eye Diseases 0.010 1.000 1 2010 2010
dbSNP: rs2286194
rs2286194 		0.925 0.040 7 81726133 intron variant T/A snv 0.19
CUI: C0022578
Disease: Keratoconus
Keratoconus 		Eye Diseases 0.010 1.000 1 2014 2014
dbSNP: rs2286194
rs2286194 		0.925 0.040 7 81726133 intron variant T/A snv 0.19
CUI: C0271183
Disease: Severe myopia
Severe myopia 		Eye Diseases 0.010 1.000 1 2009 2009
dbSNP: rs3735520
rs3735520 		0.851 0.040 7 81771623 upstream gene variant G/A;T snv
CUI: C0022578
Disease: Keratoconus
Keratoconus 		Eye Diseases 0.010 1.000 1 2015 2015
dbSNP: rs3735520
rs3735520 		0.851 0.040 7 81771623 upstream gene variant G/A;T snv
CUI: C0017605
Disease: Angle Closure Glaucoma
Angle Closure Glaucoma 		Eye Diseases 0.010 1.000 1 2013 2013
dbSNP: rs3735520
rs3735520 		0.851 0.040 7 81771623 upstream gene variant G/A;T snv
CUI: C0017606
Disease: Primary angle-closure glaucoma
Primary angle-closure glaucoma 		Eye Diseases 0.010 1.000 1 2013 2013
dbSNP: rs3735520
rs3735520 		0.851 0.040 7 81771623 upstream gene variant G/A;T snv
CUI: C0271183
Disease: Severe myopia
Severe myopia 		Eye Diseases 0.010 1.000 1 2009 2009
dbSNP: rs4732402
rs4732402 		1.000 0.040 7 81701064 3 prime UTR variant C/A;G snv
CUI: C4315867
Disease: Moderate myopia
Moderate myopia 		Eye Diseases 0.010 1.000 1 2010 2010
dbSNP: rs549654942
rs549654942 		1.000 0.080 7 81729639 missense variant C/T snv 2.0E-05 7.0E-06
CUI: C0936223
Disease: Metastatic Prostate Carcinoma
Metastatic Prostate Carcinoma 		Neoplasms; Male Urogenital Diseases 0.010 1.000 1 2013 2013