Source: ALL

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: rs773641005
rs773641005
0.742 0.240 16 58723829 missense variant T/C snv
Diabetes Mellitus, Non-Insulin-Dependent
0.060 0.667 6 1999 2017
dbSNP: rs773641005
rs773641005
0.742 0.240 16 58723829 missense variant T/C snv
CUI: C0028754
Disease: Obesity
Obesity
0.040 0.750 4 1999 2013
dbSNP: rs773641005
rs773641005
0.742 0.240 16 58723829 missense variant T/C snv
CUI: C0242339
Disease: Dyslipidemias
Dyslipidemias
0.030 1.000 3 1999 2015
dbSNP: rs773641005
rs773641005
0.742 0.240 16 58723829 missense variant T/C snv
CUI: C0524620
Disease: Metabolic Syndrome X
Metabolic Syndrome X
0.020 1.000 2 2005 2006
dbSNP: rs773641005
rs773641005
0.742 0.240 16 58723829 missense variant T/C snv
CUI: C0004153
Disease: Atherosclerosis
Atherosclerosis
0.020 1.000 2 2001 2017
dbSNP: rs773641005
rs773641005
0.742 0.240 16 58723829 missense variant T/C snv
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease
0.010 1.000 1 1998 1998
dbSNP: rs773641005
rs773641005
0.742 0.240 16 58723829 missense variant T/C snv
CUI: C0020473
Disease: Hyperlipidemia
Hyperlipidemia
0.010 < 0.001 1 2001 2001
dbSNP: rs773641005
rs773641005
0.742 0.240 16 58723829 missense variant T/C snv
CUI: C0009402
Disease: Colorectal Carcinoma
Colorectal Carcinoma
0.010 1.000 1 2013 2013
dbSNP: rs773641005
rs773641005
0.742 0.240 16 58723829 missense variant T/C snv
Malignant neoplasm of colon and/or rectum
0.010 1.000 1 2013 2013
dbSNP: rs773641005
rs773641005
0.742 0.240 16 58723829 missense variant T/C snv
CUI: C0003850
Disease: Arteriosclerosis
Arteriosclerosis
0.010 1.000 1 2017 2017
dbSNP: rs773641005
rs773641005
0.742 0.240 16 58723829 missense variant T/C snv
CUI: C0020557
Disease: Hypertriglyceridemia
Hypertriglyceridemia
0.010 1.000 1 2006 2006
dbSNP: rs773641005
rs773641005
0.742 0.240 16 58723829 missense variant T/C snv
CUI: C3714619
Disease: Insulin resistance syndrome
Insulin resistance syndrome
0.010 1.000 1 2005 2005
dbSNP: rs773641005
rs773641005
0.742 0.240 16 58723829 missense variant T/C snv
CUI: C0400966
Disease: Non-alcoholic Fatty Liver Disease
Non-alcoholic Fatty Liver Disease
0.010 1.000 1 2010 2010
dbSNP: rs773641005
rs773641005
0.742 0.240 16 58723829 missense variant T/C snv
CUI: C0271650
Disease: Impaired glucose tolerance
Impaired glucose tolerance
0.010 1.000 1 1999 1999