rs11065987, None

N. diseases: 17
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.
Low density lipoprotein cholesterol measurement
1142 0.807 0.280 12 111634620 intergenic variant A/G snv 0.29 0.800 1.000 3 2010 2018
Serum total cholesterol measurement
CUI: C1445957
Disease: Serum total cholesterol measurement
1243 0.807 0.280 12 111634620 intergenic variant A/G snv 0.29 0.800 1.000 3 2010 2018
Hematocrit procedure
CUI: C0018935
Disease: Hematocrit procedure
216 0.807 0.280 12 111634620 intergenic variant A/G snv 0.29 0.800 1.000 2 2009 2017
Hemoglobin measurement
CUI: C0518015
Disease: Hemoglobin measurement
224 0.807 0.280 12 111634620 intergenic variant A/G snv 0.29 0.800 1.000 1 2009 2009
Tetralogy of Fallot
CUI: C0039685
Disease: Tetralogy of Fallot
83 0.807 0.280 12 111634620 intergenic variant A/G snv 0.29 0.800 1.000 1 2013 2013
Body mass index
CUI: C1305855
Disease: Body mass index
2689 0.807 0.280 12 111634620 intergenic variant A/G snv 0.29 0.700 1.000 3 2015 2018
Serum LDL cholesterol measurement
CUI: C0428474
Disease: Serum LDL cholesterol measurement
555 0.807 0.280 12 111634620 intergenic variant A/G snv 0.29 0.700 1.000 2 2010 2013
Arthritis, Gouty
CUI: C0003868
Disease: Arthritis, Gouty
2356 0.807 0.280 12 111634620 intergenic variant A/G snv 0.29 0.700 1.000 1 2013 2013
Cerebrovascular accident
CUI: C0038454
Disease: Cerebrovascular accident
591 0.807 0.280 12 111634620 intergenic variant A/G snv 0.29 0.700 1.000 1 2014 2014
Coronary heart disease
CUI: C0010068
Disease: Coronary heart disease
1178 0.807 0.280 12 111634620 intergenic variant A/G snv 0.29 0.700 1.000 1 2014 2014
Corpuscular Hemoglobin Concentration Mean
4389 0.807 0.280 12 111634620 intergenic variant A/G snv 0.29 0.700 1.000 1 2012 2012
Gout
CUI: C0018099
Disease: Gout
2354 0.807 0.280 12 111634620 intergenic variant A/G snv 0.29 0.700 1.000 1 2013 2013
Hemoglobin, CTCAE
CUI: C2239101
Disease: Hemoglobin, CTCAE
26 0.807 0.280 12 111634620 intergenic variant A/G snv 0.29 0.700 1.000 1 2009 2009
High density lipoprotein measurement
1440 0.807 0.280 12 111634620 intergenic variant A/G snv 0.29 0.700 1.000 1 2018 2018
Hypothyroidism
CUI: C0020676
Disease: Hypothyroidism
283 0.807 0.280 12 111634620 intergenic variant A/G snv 0.29 0.700 1.000 1 2012 2012
Platelet mean volume determination (procedure)
371 0.807 0.280 12 111634620 intergenic variant A/G snv 0.29 0.700 1.000 1 2012 2012
Primary biliary cirrhosis
CUI: C0008312
Disease: Primary biliary cirrhosis
667 0.807 0.280 12 111634620 intergenic variant A/G snv 0.29 0.700 1.000 1 2015 2015