Source: GWASDB

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Disease Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs1532624
rs1532624
CETP
0.851 0.160 16 56971567 intron variant C/A snv 0.34
CUI: C0392885
Disease: High density lipoprotein measurement
High density lipoprotein measurement 		0.800 1.000 4 2009 2019
dbSNP: rs1532624
rs1532624
CETP
0.851 0.160 16 56971567 intron variant C/A snv 0.34
CUI: C1445957
Disease: Serum total cholesterol measurement
Serum total cholesterol measurement 		0.800 1.000 1 2010 2012
dbSNP: rs1532624
rs1532624
CETP
0.851 0.160 16 56971567 intron variant C/A snv 0.34
CUI: C0428472
Disease: Serum HDL cholesterol measurement
Serum HDL cholesterol measurement 		0.700 1.000 4 2009 2013
dbSNP: rs1532624
rs1532624
CETP
0.851 0.160 16 56971567 intron variant C/A snv 0.34
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement 		0.700 1.000 1 2012 2012
dbSNP: rs1532624
rs1532624
CETP
0.851 0.160 16 56971567 intron variant C/A snv 0.34
CUI: C0201950
Disease: Cholesterol measurement test
Cholesterol measurement test 		0.700 1.000 1 2010 2010
dbSNP: rs1532624
rs1532624
CETP
0.851 0.160 16 56971567 intron variant C/A snv 0.34
CUI: C1168443
Disease: Pseudocholinesterase Measurement
Pseudocholinesterase Measurement 		0.700 1.000 1 2011 2011
dbSNP: rs1532624
rs1532624
CETP
0.851 0.160 16 56971567 intron variant C/A snv 0.34
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease 		0.700 1.000 1 2011 2011