rs773641005, GOT2

N. diseases: 14
Source: ALL
Disease N. SNPs d DSI v DPI v Chr Position Consequence Alleles Class AFEXOME AFGENOME Score vda EI vda N. PMIDs First Ref. Last Ref.
Diabetes Mellitus, Non-Insulin-Dependent
2672 0.742 0.240 16 58723829 missense variant T/C snv 0.060 0.667 6 1999 2017
Obesity
CUI: C0028754
Disease: Obesity
1111 0.742 0.240 16 58723829 missense variant T/C snv 0.040 0.750 4 1999 2013
Dyslipidemias
CUI: C0242339
Disease: Dyslipidemias
184 0.742 0.240 16 58723829 missense variant T/C snv 0.030 1.000 3 1999 2015
Atherosclerosis
CUI: C0004153
Disease: Atherosclerosis
281 0.742 0.240 16 58723829 missense variant T/C snv 0.020 1.000 2 2001 2017
Metabolic Syndrome X
CUI: C0524620
Disease: Metabolic Syndrome X
591 0.742 0.240 16 58723829 missense variant T/C snv 0.020 1.000 2 2005 2006
Arteriosclerosis
CUI: C0003850
Disease: Arteriosclerosis
267 0.742 0.240 16 58723829 missense variant T/C snv 0.010 1.000 1 2017 2017
Colorectal Carcinoma
CUI: C0009402
Disease: Colorectal Carcinoma
1962 0.742 0.240 16 58723829 missense variant T/C snv 0.010 1.000 1 2013 2013
Coronary heart disease
CUI: C0010068
Disease: Coronary heart disease
1178 0.742 0.240 16 58723829 missense variant T/C snv 0.010 1.000 1 1998 1998
Hyperlipidemia
CUI: C0020473
Disease: Hyperlipidemia
83 0.742 0.240 16 58723829 missense variant T/C snv 0.010 1 2001 2001
Hypertriglyceridemia
CUI: C0020557
Disease: Hypertriglyceridemia
169 0.742 0.240 16 58723829 missense variant T/C snv 0.010 1.000 1 2006 2006
Impaired glucose tolerance
CUI: C0271650
Disease: Impaired glucose tolerance
81 0.742 0.240 16 58723829 missense variant T/C snv 0.010 1.000 1 1999 1999
Insulin resistance syndrome
CUI: C3714619
Disease: Insulin resistance syndrome
15 0.742 0.240 16 58723829 missense variant T/C snv 0.010 1.000 1 2005 2005
Malignant neoplasm of colon and/or rectum
502 0.742 0.240 16 58723829 missense variant T/C snv 0.010 1.000 1 2013 2013
Non-alcoholic Fatty Liver Disease
CUI: C0400966
Disease: Non-alcoholic Fatty Liver Disease
222 0.742 0.240 16 58723829 missense variant T/C snv 0.010 1.000 1 2010 2010