ZPR1, ZPR1 zinc finger, 8882

N. diseases: 64; N. variants: 35
Source: ALL
Variant DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Disease Disease Class Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs964184
rs964184 		0.716 0.440 11 116778201 3 prime UTR variant G/C snv 0.82
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease 		Cardiovascular Diseases 0.830 1.000 7 2011 2018
dbSNP: rs964184
rs964184 		0.716 0.440 11 116778201 3 prime UTR variant G/C snv 0.82
CUI: C0020557
Disease: Hypertriglyceridemia
Hypertriglyceridemia 		Nutritional and Metabolic Diseases 0.830 1.000 6 2010 2019
dbSNP: rs964184
rs964184 		0.716 0.440 11 116778201 3 prime UTR variant G/C snv 0.82
CUI: C0524620
Disease: Metabolic Syndrome X
Metabolic Syndrome X 		Nutritional and Metabolic Diseases 0.810 1.000 1 2012 2012
dbSNP: rs964184
rs964184 		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 22 2009 2019
dbSNP: rs964184
rs964184 		0.716 0.440 11 116778201 3 prime UTR variant G/C snv 0.82
CUI: C0392885
Disease: High density lipoprotein measurement
High density lipoprotein measurement 		0.800 1.000 12 2009 2019
dbSNP: rs964184
rs964184 		0.716 0.440 11 116778201 3 prime UTR variant G/C snv 0.82
CUI: C1445957
Disease: Serum total cholesterol measurement
Serum total cholesterol measurement 		0.800 1.000 9 2010 2019
dbSNP: rs964184
rs964184 		0.716 0.440 11 116778201 3 prime UTR variant G/C snv 0.82
CUI: C0202117
Disease: Low density lipoprotein cholesterol measurement
Low density lipoprotein cholesterol measurement 		0.800 1.000 6 2010 2019
dbSNP: rs2075290
rs2075290 		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: rs603446
rs603446 		1.000 0.040 11 116783719 intron variant C/T snv 0.33
CUI: C0202236
Disease: Triglycerides measurement
Triglycerides measurement 		0.800 1.000 5 2011 2019
dbSNP: rs2075290
rs2075290 		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: rs35120633
rs35120633 		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 4 2009 2019
dbSNP: rs3741298
rs3741298 		11 116786845 intron variant C/T snv 0.73
CUI: C0202236
Disease: Triglycerides measurement
Triglycerides measurement 		0.800 1.000 4 2012 2019
dbSNP: rs12286037
rs12286037 		1.000 0.040 11 116781491 intron variant C/T snv 0.11
CUI: C0202236
Disease: Triglycerides measurement
Triglycerides measurement 		0.800 1.000 3 2008 2019
dbSNP: rs2075290
rs2075290 		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: rs2160669
rs2160669 		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: rs2266788
rs2266788 		0.763 0.440 11 116789970 3 prime UTR variant G/A snv 0.93
CUI: C0392885
Disease: High density lipoprotein measurement
High density lipoprotein measurement 		0.800 1.000 3 2011 2018
dbSNP: rs2266788
rs2266788 		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 3 2011 2018
dbSNP: rs6589566
rs6589566 		0.882 0.080 11 116781707 intron variant G/A;C;T snv
CUI: C0202236
Disease: Triglycerides measurement
Triglycerides measurement 		0.800 1.000 3 2012 2019
dbSNP: rs12286037
rs12286037 		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 2 2012 2019
dbSNP: rs2266788
rs2266788 		0.763 0.440 11 116789970 3 prime UTR variant G/A snv 0.93
CUI: C1445957
Disease: Serum total cholesterol measurement
Serum total cholesterol measurement 		0.800 1.000 2 2012 2018
dbSNP: rs6589566
rs6589566 		0.882 0.080 11 116781707 intron variant G/A;C;T snv
CUI: C1445957
Disease: Serum total cholesterol measurement
Serum total cholesterol measurement 		0.800 1.000 2 2012 2019
dbSNP: rs11823543
rs11823543 		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: rs12286037
rs12286037 		1.000 0.040 11 116781491 intron variant C/T snv 0.11
CUI: C0524620
Disease: Metabolic Syndrome X
Metabolic Syndrome X 		Nutritional and Metabolic Diseases 0.800 1.000 1 2011 2011
dbSNP: rs2075290
rs2075290 		0.882 0.160 11 116782580 intron variant C/G;T snv
CUI: C0524620
Disease: Metabolic Syndrome X
Metabolic Syndrome X 		Nutritional and Metabolic Diseases 0.800 1.000 1 2011 2011
dbSNP: rs2266788
rs2266788 		0.763 0.440 11 116789970 3 prime UTR variant G/A snv 0.93
CUI: C0524620
Disease: Metabolic Syndrome X
Metabolic Syndrome X 		Nutritional and Metabolic Diseases 0.800 1.000 1 2011 2011