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: 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: 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: 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 3 2011 2019
dbSNP: rs11604424
rs11604424
ZPR1
11 116780399 intron variant C/G;T snv
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement 		0.700 1.000 1 2012 2012
dbSNP: rs2075290
rs2075290
ZPR1
0.882 0.160 11 116782580 intron variant C/G;T snv
CUI: C0524620
Disease: Metabolic Syndrome X
Metabolic Syndrome X 		0.800 1.000 1 2011 2011
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 1 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 1 2012 2019
dbSNP: rs2075290
rs2075290
ZPR1
0.882 0.160 11 116782580 intron variant C/G;T snv
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement 		0.700 1.000 1 2012 2012
dbSNP: rs2075290
rs2075290
ZPR1
0.882 0.160 11 116782580 intron variant C/G;T snv
CUI: C0428472
Disease: Serum HDL cholesterol measurement
Serum HDL cholesterol measurement 		0.700 1.000 1 2012 2012
dbSNP: rs2075290
rs2075290
ZPR1
0.882 0.160 11 116782580 intron variant C/G;T snv
CUI: C1168443
Disease: Pseudocholinesterase Measurement
Pseudocholinesterase Measurement 		0.700 1.000 1 2011 2011
dbSNP: rs12286037
rs12286037
ZPR1
1.000 0.040 11 116781491 intron variant C/T snv 0.11
CUI: C0202236
Disease: Triglycerides measurement
Triglycerides measurement 		0.800 1.000 2 2008 2019
dbSNP: rs603446
rs603446
ZPR1
1.000 0.040 11 116783719 intron variant C/T snv 0.33
CUI: C0202236
Disease: Triglycerides measurement
Triglycerides measurement 		0.800 1.000 2 2011 2019
dbSNP: rs12286037
rs12286037
ZPR1
1.000 0.040 11 116781491 intron variant C/T snv 0.11
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement 		0.700 1.000 1 2012 2012
dbSNP: rs12286037
rs12286037
ZPR1
1.000 0.040 11 116781491 intron variant C/T snv 0.11
CUI: C0428472
Disease: Serum HDL cholesterol measurement
Serum HDL cholesterol measurement 		0.700 1.000 1 2012 2012
dbSNP: rs12286037
rs12286037
ZPR1
1.000 0.040 11 116781491 intron variant C/T snv 0.11
CUI: C1445957
Disease: Serum total cholesterol measurement
Serum total cholesterol measurement 		0.700 1.000 1 2012 2012
dbSNP: rs12286037
rs12286037
ZPR1
1.000 0.040 11 116781491 intron variant C/T snv 0.11
CUI: C0392885
Disease: High density lipoprotein measurement
High density lipoprotein measurement 		0.800 1.000 1 2012 2019
dbSNP: rs12286037
rs12286037
ZPR1
1.000 0.040 11 116781491 intron variant C/T snv 0.11
CUI: C0524620
Disease: Metabolic Syndrome X
Metabolic Syndrome X 		0.800 1.000 1 2011 2011
dbSNP: rs17120029
rs17120029
ZPR1
11 116779402 intron variant C/T snv 0.11
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement 		0.700 1.000 1 2012 2012
dbSNP: rs2160669
rs2160669
ZPR1
1.000 0.040 11 116776891 3 prime UTR variant C/T snv 0.92
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement 		0.700 1.000 1 2012 2012
dbSNP: rs2160669
rs2160669
ZPR1
1.000 0.040 11 116776891 3 prime UTR variant C/T snv 0.92
CUI: C0202236
Disease: Triglycerides measurement
Triglycerides measurement 		0.800 1.000 1 2013 2019
dbSNP: rs3135507
rs3135507
ZPR1 ; APOA5
0.925 0.120 11 116790772 missense variant C/T snv 5.0E-02 5.5E-02
CUI: C0202236
Disease: Triglycerides measurement
Triglycerides measurement 		0.700 1.000 1 2012 2012
dbSNP: rs3741297
rs3741297
ZPR1
11 116786951 intron variant C/T snv 8.6E-03 1.0E-02
CUI: C1445957
Disease: Serum total cholesterol measurement
Serum total cholesterol measurement 		0.700 1.000 1 2013 2013
dbSNP: rs3741298
rs3741298
ZPR1
11 116786845 intron variant C/T snv 0.73
CUI: C0162701
Disease: Polysomnography
Polysomnography 		0.700 1.000 1 2012 2012
dbSNP: rs3741298
rs3741298
ZPR1
11 116786845 intron variant C/T snv 0.73
CUI: C0202236
Disease: Triglycerides measurement
Triglycerides measurement 		0.800 1.000 1 2012 2019