rs964184, ZPR1

N. diseases: 47
Source: ALL
Disease N. SNPs d DSI v DPI v Chr Position Consequence Alleles Class AFEXOME AFGENOME Score vda EI vda N. PMIDs First Ref. Last Ref.
Vitamin E Assay
CUI: C1142098
Disease: Vitamin E Assay
4 0.716 0.440 11 116778201 3 prime UTR variant G/C snv 0.82 0.800 1.000 1 2011 2011
Vitamin measurement
CUI: C0428580
Disease: Vitamin measurement
4 0.716 0.440 11 116778201 3 prime UTR variant G/C snv 0.82 0.700 1.000 1 2013 2013
Vitamin K Assay
CUI: C0042879
Disease: Vitamin K Assay
6 0.716 0.440 11 116778201 3 prime UTR variant G/C snv 0.82 0.700 1.000 1 2014 2014
Hyper LDL cholesterolaemia
CUI: C2242712
Disease: Hyper LDL cholesterolaemia
19 0.716 0.440 11 116778201 3 prime UTR variant G/C snv 0.82 0.010 1.000 1 2015 2015
VLDL cholesterol measurement
CUI: C0523560
Disease: VLDL cholesterol measurement
23 0.716 0.440 11 116778201 3 prime UTR variant G/C snv 0.82 0.700 1.000 1 2017 2017
Hypochondroplasia (disorder)
CUI: C0410529
Disease: Hypochondroplasia (disorder)
42 0.716 0.440 11 116778201 3 prime UTR variant G/C snv 0.82 0.010 1.000 1 2014 2014
elevated blood glucose level
CUI: C0495706
Disease: elevated blood glucose level
111 0.716 0.440 11 116778201 3 prime UTR variant G/C snv 0.82 0.700 1.000 1 2016 2016
Glucose measurement
CUI: C0337438
Disease: Glucose measurement
111 0.716 0.440 11 116778201 3 prime UTR variant G/C snv 0.82 0.700 1.000 1 2016 2016
Anemia, Sickle Cell
CUI: C0002895
Disease: Anemia, Sickle Cell
138 0.716 0.440 11 116778201 3 prime UTR variant G/C snv 0.82 0.010 1.000 1 2020 2020
Hypertriglyceridemia
CUI: C0020557
Disease: Hypertriglyceridemia
169 0.716 0.440 11 116778201 3 prime UTR variant G/C snv 0.82 0.830 1.000 6 2010 2019
Dyslipidemias
CUI: C0242339
Disease: Dyslipidemias
184 0.716 0.440 11 116778201 3 prime UTR variant G/C snv 0.82 0.020 1.000 2 2010 2013
Platelet Component Distribution Width Measurement
200 0.716 0.440 11 116778201 3 prime UTR variant G/C snv 0.82 0.700 1.000 1 2016 2016
Heart failure
CUI: C0018801
Disease: Heart failure
201 0.716 0.440 11 116778201 3 prime UTR variant G/C snv 0.82 0.700 1.000 1 2016 2016
Calcification of coronary artery
CUI: C1611184
Disease: Calcification of coronary artery
205 0.716 0.440 11 116778201 3 prime UTR variant G/C snv 0.82 0.700 1.000 1 2012 2012
Hematocrit procedure
CUI: C0018935
Disease: Hematocrit procedure
216 0.716 0.440 11 116778201 3 prime UTR variant G/C snv 0.82 0.700 1.000 1 2016 2016
Phospholipid measurement
CUI: C0202177
Disease: Phospholipid measurement
306 0.716 0.440 11 116778201 3 prime UTR variant G/C snv 0.82 0.800 1.000 1 2012 2012
Platelet mean volume determination (procedure)
371 0.716 0.440 11 116778201 3 prime UTR variant G/C snv 0.82 0.700 1.000 1 2016 2016
Coronary Arteriosclerosis
CUI: C0010054
Disease: Coronary Arteriosclerosis
440 0.716 0.440 11 116778201 3 prime UTR variant G/C snv 0.82 0.020 1.000 2 2013 2018
Reticulocyte count (procedure)
CUI: C0206161
Disease: Reticulocyte count (procedure)
474 0.716 0.440 11 116778201 3 prime UTR variant G/C snv 0.82 0.700 1.000 1 2016 2016
Serum LDL cholesterol measurement
CUI: C0428474
Disease: Serum LDL cholesterol measurement
555 0.716 0.440 11 116778201 3 prime UTR variant G/C snv 0.82 0.700 1.000 2 2010 2013
Pseudocholinesterase Measurement
CUI: C1168443
Disease: Pseudocholinesterase Measurement
568 0.716 0.440 11 116778201 3 prime UTR variant G/C snv 0.82 0.700 1.000 1 2011 2011
Atrial Fibrillation
CUI: C0004238
Disease: Atrial Fibrillation
584 0.716 0.440 11 116778201 3 prime UTR variant G/C snv 0.82 0.700 1.000 1 2016 2016
Cerebrovascular accident
CUI: C0038454
Disease: Cerebrovascular accident
591 0.716 0.440 11 116778201 3 prime UTR variant G/C snv 0.82 0.700 1.000 1 2016 2016
Metabolic Syndrome X
CUI: C0524620
Disease: Metabolic Syndrome X
591 0.716 0.440 11 116778201 3 prime UTR variant G/C snv 0.82 0.810 1.000 1 2012 2012
Serum HDL cholesterol measurement
CUI: C0428472
Disease: Serum HDL cholesterol measurement
679 0.716 0.440 11 116778201 3 prime UTR variant G/C snv 0.82 0.700 1.000 6 2009 2013