Source: GWASDB

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: rs12287066
rs12287066
APOA5
11 116791615 synonymous variant G/T snv 7.7E-02 0.10
CUI: C0202236
Disease: Triglycerides measurement
Triglycerides measurement 		0.700 1.000 2 2012 2012
dbSNP: rs9804646
rs9804646
APOA5
11 116794363 upstream gene variant C/T snv 0.17
CUI: C0202236
Disease: Triglycerides measurement
Triglycerides measurement 		0.800 1.000 2 2012 2019
dbSNP: rs12287066
rs12287066
APOA5
11 116791615 synonymous variant G/T snv 7.7E-02 0.10
CUI: C1445957
Disease: Serum total cholesterol measurement
Serum total cholesterol measurement 		0.700 1.000 1 2012 2012
dbSNP: rs12287066
rs12287066
APOA5
11 116791615 synonymous variant G/T snv 7.7E-02 0.10
CUI: C0428472
Disease: Serum HDL cholesterol measurement
Serum HDL cholesterol measurement 		0.700 1.000 1 2012 2012
dbSNP: rs12287066
rs12287066
APOA5
11 116791615 synonymous variant G/T snv 7.7E-02 0.10
CUI: C0392885
Disease: High density lipoprotein measurement
High density lipoprotein measurement 		0.700 1.000 1 2012 2012
dbSNP: rs2072560
rs2072560
ZPR1 ; APOA5
11 116791110 missense variant T/C snv 0.89 0.94
CUI: C1445957
Disease: Serum total cholesterol measurement
Serum total cholesterol measurement 		0.700 1.000 1 2012 2012
dbSNP: rs2072560
rs2072560
ZPR1 ; APOA5
11 116791110 missense variant T/C snv 0.89 0.94
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement 		0.700 1.000 1 2012 2012
dbSNP: rs2072560
rs2072560
ZPR1 ; APOA5
11 116791110 missense variant T/C snv 0.89 0.94
CUI: C0428472
Disease: Serum HDL cholesterol measurement
Serum HDL cholesterol measurement 		0.700 1.000 1 2012 2012
dbSNP: rs2072560
rs2072560
ZPR1 ; APOA5
11 116791110 missense variant T/C snv 0.89 0.94
CUI: C0392885
Disease: High density lipoprotein measurement
High density lipoprotein measurement 		0.700 1.000 1 2012 2012
dbSNP: rs2072560
rs2072560
ZPR1 ; APOA5
11 116791110 missense variant T/C snv 0.89 0.94
CUI: C0202236
Disease: Triglycerides measurement
Triglycerides measurement 		0.700 1.000 1 2012 2012
dbSNP: rs34003087
rs34003087
APOA5
11 116792880 upstream gene variant C/T snv 4.7E-02
CUI: C0202236
Disease: Triglycerides measurement
Triglycerides measurement 		0.700 1.000 1 2012 2012
dbSNP: rs34003087
rs34003087
APOA5
11 116792880 upstream gene variant C/T snv 4.7E-02
CUI: C0428472
Disease: Serum HDL cholesterol measurement
Serum HDL cholesterol measurement 		0.700 1.000 1 2012 2012
dbSNP: rs34003087
rs34003087
APOA5
11 116792880 upstream gene variant C/T snv 4.7E-02
CUI: C0392885
Disease: High density lipoprotein measurement
High density lipoprotein measurement 		0.700 1.000 1 2012 2012
dbSNP: rs619054
rs619054
ZPR1 ; APOA5
11 116790097 3 prime UTR variant G/A snv 0.19 0.19
CUI: C0202236
Disease: Triglycerides measurement
Triglycerides measurement 		0.700 1.000 1 2012 2012
dbSNP: rs7103224
rs7103224
APOA5
11 116793250 upstream gene variant G/A snv 5.8E-02
CUI: C0202236
Disease: Triglycerides measurement
Triglycerides measurement 		0.700 1.000 1 2012 2012
dbSNP: rs7103224
rs7103224
APOA5
11 116793250 upstream gene variant G/A snv 5.8E-02
CUI: C1445957
Disease: Serum total cholesterol measurement
Serum total cholesterol measurement 		0.700 1.000 1 2012 2012
dbSNP: rs9804646
rs9804646
APOA5
11 116794363 upstream gene variant C/T snv 0.17
CUI: C1445957
Disease: Serum total cholesterol measurement
Serum total cholesterol measurement 		0.800 1.000 1 2012 2018
dbSNP: rs662799
rs662799
APOA5
0.689 0.480 11 116792991 upstream gene variant G/A snv 0.90
CUI: C0428472
Disease: Serum HDL cholesterol measurement
Serum HDL cholesterol measurement 		0.700 1.000 2 2012 2012
dbSNP: rs662799
rs662799
APOA5
0.689 0.480 11 116792991 upstream gene variant G/A snv 0.90
CUI: C0202236
Disease: Triglycerides measurement
Triglycerides measurement 		0.800 1.000 2 2012 2019
dbSNP: rs662799
rs662799
APOA5
0.689 0.480 11 116792991 upstream gene variant G/A snv 0.90
CUI: C0392885
Disease: High density lipoprotein measurement
High density lipoprotein measurement 		0.800 1.000 2 2012 2019
dbSNP: rs662799
rs662799
APOA5
0.689 0.480 11 116792991 upstream gene variant G/A snv 0.90
CUI: C1445957
Disease: Serum total cholesterol measurement
Serum total cholesterol measurement 		0.800 1.000 2 2012 2019
dbSNP: rs662799
rs662799
APOA5
0.689 0.480 11 116792991 upstream gene variant G/A snv 0.90
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement 		0.700 1.000 1 2012 2012
dbSNP: rs662799
rs662799
APOA5
0.689 0.480 11 116792991 upstream gene variant G/A snv 0.90
CUI: C0162701
Disease: Polysomnography
Polysomnography 		0.700 1.000 1 2012 2012
dbSNP: rs3135506
rs3135506
APOA5
0.708 0.400 11 116791691 missense variant G/A;C snv 3.0E-05; 6.8E-02
CUI: C0202236
Disease: Triglycerides measurement
Triglycerides measurement 		0.800 1.000 2 2009 2019
dbSNP: rs2266788
rs2266788
ZPR1 ; APOA5
0.763 0.440 11 116789970 3 prime UTR variant G/A snv 0.93
CUI: C0202236
Disease: Triglycerides measurement
Triglycerides measurement 		0.800 1.000 2 2011 2018