rs4810479, None

N. diseases: 7
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.
High density lipoprotein measurement
1440 1.000 0.040 20 45916409 upstream gene variant C/T snv 0.68 0.800 1.000 3 2012 2018
Triglycerides measurement
CUI: C0202236
Disease: Triglycerides measurement
1418 1.000 0.040 20 45916409 upstream gene variant C/T snv 0.68 0.800 1.000 2 2012 2018
Serum HDL cholesterol measurement
CUI: C0428472
Disease: Serum HDL cholesterol measurement
679 1.000 0.040 20 45916409 upstream gene variant C/T snv 0.68 0.700 1.000 2 2012 2012
Calcification of coronary artery
CUI: C1611184
Disease: Calcification of coronary artery
205 1.000 0.040 20 45916409 upstream gene variant C/T snv 0.68 0.700 1.000 1 2012 2012
Serum albumin measurement
CUI: C0523465
Disease: Serum albumin measurement
3282 1.000 0.040 20 45916409 upstream gene variant C/T snv 0.68 0.700 1.000 1 2012 2012
Diabetes
CUI: C0011847
Disease: Diabetes
710 1.000 0.040 20 45916409 upstream gene variant C/T snv 0.68 0.010 1.000 1 2015 2015
Diabetes Mellitus
CUI: C0011849
Disease: Diabetes Mellitus
824 1.000 0.040 20 45916409 upstream gene variant C/T snv 0.68 0.010 1.000 1 2015 2015