rs662799, APOA5

N. diseases: 7
Source: CURATED ×
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 0.689 0.480 11 116792991 upstream gene variant G/A snv 0.90 0.800 1.000 8 2012 2019
High density lipoprotein measurement
CUI: C0392885
Disease: High density lipoprotein measurement
1440 0.689 0.480 11 116792991 upstream gene variant G/A snv 0.90 0.800 1.000 7 2012 2019
Serum total cholesterol measurement
CUI: C1445957
Disease: Serum total cholesterol measurement
1243 0.689 0.480 11 116792991 upstream gene variant G/A snv 0.90 0.800 1.000 3 2012 2019
Serum HDL cholesterol measurement
CUI: C0428472
Disease: Serum HDL cholesterol measurement
679 0.689 0.480 11 116792991 upstream gene variant G/A snv 0.90 0.700 1.000 2 2012 2012
Platelet Count measurement
CUI: C0032181
Disease: Platelet Count measurement
457 0.689 0.480 11 116792991 upstream gene variant G/A snv 0.90 0.700 1.000 1 2018 2018
Polysomnography
CUI: C0162701
Disease: Polysomnography
249 0.689 0.480 11 116792991 upstream gene variant G/A snv 0.90 0.700 1.000 1 2012 2012
Serum albumin measurement
CUI: C0523465
Disease: Serum albumin measurement
3282 0.689 0.480 11 116792991 upstream gene variant G/A snv 0.90 0.700 1.000 1 2012 2012