rs17145750, MLXIPL

N. diseases: 9
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.
Serum gamma-glutamyl transferase measurement
CUI: C1278049
Disease: Serum gamma-glutamyl transferase measurement
108 0.925 0.120 7 73612048 intron variant C/A;T snv 0.800 1.000 1 2011 2011
Triglycerides measurement
CUI: C0202236
Disease: Triglycerides measurement
1418 0.925 0.120 7 73612048 intron variant C/A;T snv 0.700 1.000 2 2012 2012
Arthritis, Gouty
CUI: C0003868
Disease: Arthritis, Gouty
2356 0.925 0.120 7 73612048 intron variant C/A;T snv 0.700 1.000 1 2013 2013
Gout
CUI: C0018099
Disease: Gout
2354 0.925 0.120 7 73612048 intron variant C/A;T snv 0.700 1.000 1 2013 2013
High density lipoprotein measurement
CUI: C0392885
Disease: High density lipoprotein measurement
1440 0.925 0.120 7 73612048 intron variant C/A;T snv 0.700 1.000 1 2012 2012
Platelet Count measurement
CUI: C0032181
Disease: Platelet Count measurement
457 0.925 0.120 7 73612048 intron variant C/A;T snv 0.700 1.000 1 2016 2016
Serum albumin measurement
CUI: C0523465
Disease: Serum albumin measurement
3282 0.925 0.120 7 73612048 intron variant C/A;T snv 0.700 1.000 1 2012 2012
Serum HDL cholesterol measurement
CUI: C0428472
Disease: Serum HDL cholesterol measurement
679 0.925 0.120 7 73612048 intron variant C/A;T snv 0.700 1.000 1 2012 2012
Uric acid measurement (procedure)
CUI: C0202239
Disease: Uric acid measurement (procedure)
1463 0.925 0.120 7 73612048 intron variant C/A;T snv 0.700 1.000 1 2019 2019