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: rs7926960
rs7926960
ZPR1
11 116783370 intron variant A/C snv 1.5E-02
CUI: C0202236
Disease: Triglycerides measurement
Triglycerides measurement 		0.700 1.000 1 2012 2012
dbSNP: rs618923
rs618923
ZPR1
11 116783443 intron variant A/G snv 0.20
CUI: C0202236
Disease: Triglycerides measurement
Triglycerides measurement 		0.700 1.000 1 2012 2012
dbSNP: rs7483863
rs7483863
ZPR1
11 116781775 intron variant A/G snv 0.93
CUI: C0392885
Disease: High density lipoprotein measurement
High density lipoprotein measurement 		0.700 1.000 1 2018 2018
dbSNP: rs10750096
rs10750096
ZPR1
11 116786072 intron variant C/A snv 0.92
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement 		0.700 1.000 1 2012 2012
dbSNP: rs2075291
rs2075291
ZPR1 ; APOA5
0.752 0.400 11 116790676 missense variant C/A;T snv 6.4E-03; 4.0E-06
CUI: C0020557
Disease: Hypertriglyceridemia
Hypertriglyceridemia 		0.080 1.000 8 2003 2018
dbSNP: rs2075291
rs2075291
ZPR1 ; APOA5
0.752 0.400 11 116790676 missense variant C/A;T snv 6.4E-03; 4.0E-06
CUI: C0392885
Disease: High density lipoprotein measurement
High density lipoprotein measurement 		0.700 1.000 3 2018 2019
dbSNP: rs2075291
rs2075291
ZPR1 ; APOA5
0.752 0.400 11 116790676 missense variant C/A;T snv 6.4E-03; 4.0E-06
CUI: C0524620
Disease: Metabolic Syndrome X
Metabolic Syndrome X 		0.720 1.000 3 2008 2019
dbSNP: rs2075291
rs2075291
ZPR1 ; APOA5
0.752 0.400 11 116790676 missense variant C/A;T snv 6.4E-03; 4.0E-06
CUI: C0202236
Disease: Triglycerides measurement
Triglycerides measurement 		0.700 1.000 3 2018 2019
dbSNP: rs2075291
rs2075291
ZPR1 ; APOA5
0.752 0.400 11 116790676 missense variant C/A;T snv 6.4E-03; 4.0E-06
CUI: C0027051
Disease: Myocardial Infarction
Myocardial Infarction 		0.020 1.000 2 2005 2016
dbSNP: rs2075291
rs2075291
ZPR1 ; APOA5
0.752 0.400 11 116790676 missense variant C/A;T snv 6.4E-03; 4.0E-06
CUI: C1956346
Disease: Coronary Artery Disease
Coronary Artery Disease 		0.720 1.000 2 2017 2019
dbSNP: rs2075291
rs2075291
ZPR1 ; APOA5
0.752 0.400 11 116790676 missense variant C/A;T snv 6.4E-03; 4.0E-06
CUI: C0004153
Disease: Atherosclerosis
Atherosclerosis 		0.020 1.000 2 2009 2018
dbSNP: rs2075291
rs2075291
ZPR1 ; APOA5
0.752 0.400 11 116790676 missense variant C/A;T snv 6.4E-03; 4.0E-06
CUI: C0003850
Disease: Arteriosclerosis
Arteriosclerosis 		0.020 1.000 2 2009 2018
dbSNP: rs2075291
rs2075291
ZPR1 ; APOA5
0.752 0.400 11 116790676 missense variant C/A;T snv 6.4E-03; 4.0E-06
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease 		0.010 1.000 1 2013 2013
dbSNP: rs2075291
rs2075291
ZPR1 ; APOA5
0.752 0.400 11 116790676 missense variant C/A;T snv 6.4E-03; 4.0E-06
CUI: C0242339
Disease: Dyslipidemias
Dyslipidemias 		0.010 1.000 1 2012 2012
dbSNP: rs2075291
rs2075291
ZPR1 ; APOA5
0.752 0.400 11 116790676 missense variant C/A;T snv 6.4E-03; 4.0E-06
CUI: C0948008
Disease: Ischemic stroke
Ischemic stroke 		0.010 1.000 1 2012 2012
dbSNP: rs2075291
rs2075291
ZPR1 ; APOA5
0.752 0.400 11 116790676 missense variant C/A;T snv 6.4E-03; 4.0E-06
CUI: C0577631
Disease: Carotid Atherosclerosis
Carotid Atherosclerosis 		0.010 1.000 1 2009 2009
dbSNP: rs2075291
rs2075291
ZPR1 ; APOA5
0.752 0.400 11 116790676 missense variant C/A;T snv 6.4E-03; 4.0E-06
CUI: C0011860
Disease: Diabetes Mellitus, Non-Insulin-Dependent
Diabetes Mellitus, Non-Insulin-Dependent 		0.010 < 0.001 1 2006 2006
dbSNP: rs2075291
rs2075291
ZPR1 ; APOA5
0.752 0.400 11 116790676 missense variant C/A;T snv 6.4E-03; 4.0E-06
CUI: C0948242
Disease: Nuchal bleb, familial
Nuchal bleb, familial 		0.010 1.000 1 2010 2010
dbSNP: rs7118999
rs7118999
ZPR1 ; BUD13
1.000 0.040 11 116774559 3 prime UTR variant C/A;T snv
CUI: C0524620
Disease: Metabolic Syndrome X
Metabolic Syndrome X 		0.010 1.000 1 2017 2017
dbSNP: rs2075291
rs2075291
ZPR1 ; APOA5
0.752 0.400 11 116790676 missense variant C/A;T snv 6.4E-03; 4.0E-06
CUI: C4016963
Disease: HYPERTRIGLYCERIDEMIA, SUSCEPTIBILITY TO
HYPERTRIGLYCERIDEMIA, SUSCEPTIBILITY TO 		0.700 0
dbSNP: rs2075290
rs2075290
ZPR1
0.882 0.160 11 116782580 intron variant C/G;T snv
CUI: C0202236
Disease: Triglycerides measurement
Triglycerides measurement 		0.800 1.000 5 2011 2019
dbSNP: rs2075290
rs2075290
ZPR1
0.882 0.160 11 116782580 intron variant C/G;T snv
CUI: C0392885
Disease: High density lipoprotein measurement
High density lipoprotein measurement 		0.800 1.000 4 2011 2019
dbSNP: rs2075290
rs2075290
ZPR1
0.882 0.160 11 116782580 intron variant C/G;T snv
CUI: C1445957
Disease: Serum total cholesterol measurement
Serum total cholesterol measurement 		0.800 1.000 3 2012 2019
dbSNP: rs11604424
rs11604424
ZPR1
11 116780399 intron variant C/G;T snv
CUI: C0202236
Disease: Triglycerides measurement
Triglycerides measurement 		0.700 1.000 2 2018 2019
dbSNP: rs11604424
rs11604424
ZPR1
11 116780399 intron variant C/G;T snv
CUI: C1445957
Disease: Serum total cholesterol measurement
Serum total cholesterol measurement 		0.700 1.000 2 2018 2019