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: C0201950
Disease: Cholesterol measurement test
Cholesterol measurement test 		0.700 1.000 1 2010 2010
dbSNP: rs7499892
rs7499892
CETP
16 56972678 intron variant C/G;T snv
CUI: C0392885
Disease: High density lipoprotein measurement
High density lipoprotein measurement 		0.800 1.000 4 2011 2019
dbSNP: rs7499892
rs7499892
CETP
16 56972678 intron variant C/G;T snv
CUI: C0428472
Disease: Serum HDL cholesterol measurement
Serum HDL cholesterol measurement 		0.700 1.000 4 2011 2012
dbSNP: rs4784744
rs4784744
CETP
16 56977273 non coding transcript exon variant G/A snv 0.30
CUI: C0428472
Disease: Serum HDL cholesterol measurement
Serum HDL cholesterol measurement 		0.700 1.000 2 2011 2012
dbSNP: rs4784744
rs4784744
CETP
16 56977273 non coding transcript exon variant G/A snv 0.30
CUI: C0392885
Disease: High density lipoprotein measurement
High density lipoprotein measurement 		0.700 1.000 2 2011 2012
dbSNP: rs708272
rs708272
CETP
0.708 0.440 16 56962376 intron variant G/A snv 0.42 0.38
CUI: C0428472
Disease: Serum HDL cholesterol measurement
Serum HDL cholesterol measurement 		0.700 1.000 2 2011 2012
dbSNP: rs708272
rs708272
CETP
0.708 0.440 16 56962376 intron variant G/A snv 0.42 0.38
CUI: C0392885
Disease: High density lipoprotein measurement
High density lipoprotein measurement 		0.700 1.000 2 2011 2012
dbSNP: rs11076175
rs11076175
CETP
16 56972466 intron variant A/G snv 0.20
CUI: C1168443
Disease: Pseudocholinesterase Measurement
Pseudocholinesterase Measurement 		0.700 1.000 1 2011 2011
dbSNP: rs11508026
rs11508026
CETP
16 56965416 intron variant C/T snv 0.32
CUI: C1168443
Disease: Pseudocholinesterase Measurement
Pseudocholinesterase Measurement 		0.700 1.000 1 2011 2011
dbSNP: rs12708980
rs12708980
CETP
16 56978467 intron variant T/G snv 0.36
CUI: C0392885
Disease: High density lipoprotein measurement
High density lipoprotein measurement 		0.800 1.000 1 2011 2019
dbSNP: rs12708980
rs12708980
CETP
16 56978467 intron variant T/G snv 0.36
CUI: C0428472
Disease: Serum HDL cholesterol measurement
Serum HDL cholesterol 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
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: rs1800775
rs1800775
CETP
0.790 0.240 16 56961324 upstream gene variant C/A;G snv 0.51; 5.7E-06
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease 		0.700 1.000 1 2011 2011
dbSNP: rs1800775
rs1800775
CETP
0.790 0.240 16 56961324 upstream gene variant C/A;G snv 0.51; 5.7E-06
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: 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: C0010068
Disease: Coronary heart disease
Coronary heart disease 		0.700 1.000 1 2011 2011
dbSNP: rs289714
rs289714
CETP
16 56973539 intron variant G/A snv 0.76; 4.0E-06 0.70
CUI: C1168443
Disease: Pseudocholinesterase Measurement
Pseudocholinesterase Measurement 		0.700 1.000 1 2011 2011
dbSNP: rs289744
rs289744
CETP
16 56984190 downstream gene variant G/T snv 0.61
CUI: C0428472
Disease: Serum HDL cholesterol measurement
Serum HDL cholesterol measurement 		0.700 1.000 1 2011 2011
dbSNP: rs289744
rs289744
CETP
16 56984190 downstream gene variant G/T snv 0.61
CUI: C0392885
Disease: High density lipoprotein measurement
High density lipoprotein measurement 		0.700 1.000 1 2011 2011
dbSNP: rs711752
rs711752
CETP
1.000 0.040 16 56962299 splice region variant G/A;C snv
CUI: C1168443
Disease: Pseudocholinesterase Measurement
Pseudocholinesterase Measurement 		0.700 1.000 1 2011 2011
dbSNP: rs7203984
rs7203984
CETP
16 56965346 intron variant A/C snv 0.31
CUI: C1168443
Disease: Pseudocholinesterase Measurement
Pseudocholinesterase Measurement 		0.700 1.000 1 2011 2011
dbSNP: rs7499892
rs7499892
CETP
16 56972678 intron variant C/G;T snv
CUI: C1168443
Disease: Pseudocholinesterase Measurement
Pseudocholinesterase Measurement 		0.700 1.000 1 2011 2011
dbSNP: rs9939224
rs9939224
CETP
1.000 0.040 16 56968820 intron variant T/G snv 0.75
CUI: C0524620
Disease: Metabolic Syndrome X
Metabolic Syndrome X 		0.800 1.000 1 2011 2011
dbSNP: rs9939224
rs9939224
CETP
1.000 0.040 16 56968820 intron variant T/G snv 0.75
CUI: C1168443
Disease: Pseudocholinesterase Measurement
Pseudocholinesterase Measurement 		0.700 1.000 1 2011 2011