Source: GWASCAT

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: rs964184
rs964184
ZPR1
0.716 0.440 11 116778201 3 prime UTR variant G/C snv 0.82
CUI: C0202236
Disease: Triglycerides measurement
Triglycerides measurement 		0.800 1.000 20 2009 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 4 2011 2019
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: 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 3 2013 2019
dbSNP: rs3741298
rs3741298
ZPR1
11 116786845 intron variant C/T snv 0.73
CUI: C0202236
Disease: Triglycerides measurement
Triglycerides measurement 		0.800 1.000 3 2012 2019
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: 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
dbSNP: rs35120633
rs35120633
ZPR1
11 116784884 missense variant G/A;C snv 6.6E-02; 8.0E-06
CUI: C0202236
Disease: Triglycerides measurement
Triglycerides measurement 		0.800 1.000 2 2009 2019
dbSNP: rs6589566
rs6589566
ZPR1
0.882 0.080 11 116781707 intron variant G/A;C;T snv
CUI: C0202236
Disease: Triglycerides measurement
Triglycerides measurement 		0.800 1.000 2 2012 2019
dbSNP: rs11823543
rs11823543
ZPR1
11 116778419 3 prime UTR variant G/A snv 0.11
CUI: C0202236
Disease: Triglycerides measurement
Triglycerides measurement 		0.800 1.000 1 2011 2011
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: 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: rs75198898
rs75198898
ZPR1
11 116779090 intron variant G/A snv 7.2E-03 4.3E-03
CUI: C0202236
Disease: Triglycerides measurement
Triglycerides measurement 		0.700 1.000 1 2018 2018