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: rs1800775
rs1800775
CETP
0.790 0.240 16 56961324 upstream gene variant C/A;G snv 0.51; 5.7E-06
CUI: C0428472
Disease: Serum HDL cholesterol measurement
Serum HDL cholesterol measurement 		0.700 1.000 5 2008 2013
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: rs5880
rs5880
CETP
0.827 0.040 16 56981179 missense variant G/C snv 5.2E-02 3.7E-02
CUI: C0428472
Disease: Serum HDL cholesterol measurement
Serum HDL cholesterol measurement 		0.700 1.000 4 2008 2014
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: 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: rs4783961
rs4783961
CETP
0.851 0.320 16 56960982 upstream gene variant G/A snv 0.48 0.47
CUI: C0428472
Disease: Serum HDL cholesterol measurement
Serum HDL cholesterol measurement 		0.700 1.000 3 2012 2012
dbSNP: rs5882
rs5882
CETP
0.649 0.400 16 56982180 missense variant G/A;C snv 0.62
CUI: C0428472
Disease: Serum HDL cholesterol measurement
Serum HDL cholesterol measurement 		0.700 1.000 3 2008 2012
dbSNP: rs5882
rs5882
CETP
0.649 0.400 16 56982180 missense variant G/A;C snv 0.62
CUI: C0392885
Disease: High density lipoprotein measurement
High density lipoprotein measurement 		0.700 1.000 3 2008 2012
dbSNP: rs711752
rs711752
CETP
1.000 0.040 16 56962299 splice region variant G/A;C snv
CUI: C0428472
Disease: Serum HDL cholesterol measurement
Serum HDL cholesterol measurement 		0.700 1.000 3 2008 2013
dbSNP: rs11076176
rs11076176
CETP
16 56973534 intron variant T/A;G snv 2.4E-05; 0.22
CUI: C0392885
Disease: High density lipoprotein measurement
High density lipoprotein measurement 		0.700 1.000 2 2012 2012
dbSNP: rs11076176
rs11076176
CETP
16 56973534 intron variant T/A;G snv 2.4E-05; 0.22
CUI: C0428472
Disease: Serum HDL cholesterol measurement
Serum HDL cholesterol measurement 		0.700 1.000 2 2012 2012
dbSNP: rs17231506
rs17231506
CETP
0.851 0.040 16 56960616 upstream gene variant C/G;T snv 0.28
CUI: C0428472
Disease: Serum HDL cholesterol measurement
Serum HDL cholesterol measurement 		0.700 1.000 2 2012 2012
dbSNP: rs17231520
rs17231520
CETP
0.851 0.240 16 56961915 upstream gene variant G/A snv 2.1E-02
CUI: C0428472
Disease: Serum HDL cholesterol measurement
Serum HDL cholesterol measurement 		0.700 1.000 2 2012 2012
dbSNP: rs1800775
rs1800775
CETP
0.790 0.240 16 56961324 upstream gene variant C/A;G snv 0.51; 5.7E-06
CUI: C0202236
Disease: Triglycerides measurement
Triglycerides measurement 		0.700 1.000 2 2007 2009
dbSNP: rs1800777
rs1800777
CETP
0.724 0.280 16 56983407 missense variant G/A snv 3.7E-02 2.8E-02
CUI: C0428472
Disease: Serum HDL cholesterol measurement
Serum HDL cholesterol measurement 		0.700 1.000 2 2008 2012
dbSNP: rs1800777
rs1800777
CETP
0.724 0.280 16 56983407 missense variant G/A snv 3.7E-02 2.8E-02
CUI: C0392885
Disease: High density lipoprotein measurement
High density lipoprotein measurement 		0.700 1.000 2 2008 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: rs5883
rs5883
CETP
1.000 0.040 16 56973441 synonymous variant C/T snv 5.1E-02 6.6E-02
CUI: C0428472
Disease: Serum HDL cholesterol measurement
Serum HDL cholesterol measurement 		0.700 1.000 2 2012 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: rs11076174
rs11076174
CETP
16 56969234 intron variant T/C snv 0.10
CUI: C0428472
Disease: Serum HDL cholesterol measurement
Serum HDL cholesterol measurement 		0.700 1.000 1 2012 2012
dbSNP: rs11076175
rs11076175
CETP
16 56972466 intron variant A/G snv 0.20
CUI: C0428472
Disease: Serum HDL cholesterol measurement
Serum HDL cholesterol measurement 		0.700 1.000 1 2012 2012
dbSNP: rs11076175
rs11076175
CETP
16 56972466 intron variant A/G snv 0.20
CUI: C0392885
Disease: High density lipoprotein measurement
High density lipoprotein measurement 		0.700 1.000 1 2012 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