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: rs1864163
rs1864163
CETP
0.882 0.120 16 56963321 intron variant G/A snv 0.26
CUI: C0242383
Disease: Age related macular degeneration
Age related macular degeneration 		0.810 1.000 1 2013 2019
dbSNP: rs1864163
rs1864163
CETP
0.882 0.120 16 56963321 intron variant G/A snv 0.26
CUI: C0392885
Disease: High density lipoprotein measurement
High density lipoprotein measurement 		0.800 1.000 3 2008 2019
dbSNP: rs1864163
rs1864163
CETP
0.882 0.120 16 56963321 intron variant G/A snv 0.26
CUI: C1445957
Disease: Serum total cholesterol measurement
Serum total cholesterol measurement 		0.800 1.000 1 2012 2019
dbSNP: rs1864163
rs1864163
CETP
0.882 0.120 16 56963321 intron variant G/A snv 0.26
CUI: C0428472
Disease: Serum HDL cholesterol measurement
Serum HDL cholesterol measurement 		0.700 1.000 3 2008 2012
dbSNP: rs1864163
rs1864163
CETP
0.882 0.120 16 56963321 intron variant G/A snv 0.26
CUI: C1168443
Disease: Pseudocholinesterase Measurement
Pseudocholinesterase Measurement 		0.700 1.000 1 2011 2011
dbSNP: rs1864163
rs1864163
CETP
0.882 0.120 16 56963321 intron variant G/A snv 0.26
CUI: C0202236
Disease: Triglycerides measurement
Triglycerides measurement 		0.700 1.000 1 2009 2009
dbSNP: rs1864163
rs1864163
CETP
0.882 0.120 16 56963321 intron variant G/A snv 0.26
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease 		0.700 1.000 1 2011 2011
dbSNP: rs1864163
rs1864163
CETP
0.882 0.120 16 56963321 intron variant G/A snv 0.26
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement 		0.700 1.000 1 2012 2012