rs2075290, ZPR1

N. diseases: 10
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.
Triglycerides measurement
CUI: C0202236
Disease: Triglycerides measurement
1418 0.882 0.160 11 116782580 intron variant C/G;T snv 0.800 1.000 5 2011 2019
High density lipoprotein measurement
1440 0.882 0.160 11 116782580 intron variant C/G;T snv 0.800 1.000 4 2011 2019
Serum total cholesterol measurement
CUI: C1445957
Disease: Serum total cholesterol measurement
1243 0.882 0.160 11 116782580 intron variant C/G;T snv 0.800 1.000 3 2012 2019
Metabolic Syndrome X
CUI: C0524620
Disease: Metabolic Syndrome X
591 0.882 0.160 11 116782580 intron variant C/G;T snv 0.800 1.000 1 2011 2011
Low density lipoprotein cholesterol measurement
1142 0.882 0.160 11 116782580 intron variant C/G;T snv 0.700 1.000 1 2018 2018
Pseudocholinesterase Measurement
CUI: C1168443
Disease: Pseudocholinesterase Measurement
568 0.882 0.160 11 116782580 intron variant C/G;T snv 0.700 1.000 1 2011 2011
Serum albumin measurement
CUI: C0523465
Disease: Serum albumin measurement
3282 0.882 0.160 11 116782580 intron variant C/G;T snv 0.700 1.000 1 2012 2012
Serum HDL cholesterol measurement
CUI: C0428472
Disease: Serum HDL cholesterol measurement
679 0.882 0.160 11 116782580 intron variant C/G;T snv 0.700 1.000 1 2012 2012
Diabetes Mellitus, Non-Insulin-Dependent
2672 0.882 0.160 11 116782580 intron variant C/G;T snv 0.010 1.000 1 2016 2016
Hypochondroplasia (disorder)
CUI: C0410529
Disease: Hypochondroplasia (disorder)
42 0.882 0.160 11 116782580 intron variant C/G;T snv 0.010 1.000 1 2014 2014