Source: CURATED

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Disease Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs5745687
rs5745687
HGF
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
HGF
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
HGF
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
HGF
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
HGF
0.925 0.120 7 81720096 intron variant T/C snv 0.85
CUI: C0018099
Disease: Gout
Gout 		0.700 1.000 1 2012 2012
dbSNP: rs5745709
rs5745709
HGF
0.925 0.120 7 81720096 intron variant T/C snv 0.85
CUI: C0003868
Disease: Arthritis, Gouty
Arthritis, Gouty 		0.700 1.000 1 2012 2012
dbSNP: rs984534
rs984534
HGF
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
HGF
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) 		0.700 0