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: 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: C0392885
Disease: High density lipoprotein measurement
High density lipoprotein measurement 		0.800 1.000 1 2012 2018
dbSNP: rs9939224
rs9939224
CETP
1.000 0.040 16 56968820 intron variant T/G snv 0.75
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement 		0.700 1.000 1 2012 2012
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
dbSNP: rs9939224
rs9939224
CETP
1.000 0.040 16 56968820 intron variant T/G snv 0.75
CUI: C1445957
Disease: Serum total cholesterol measurement
Serum total cholesterol measurement 		0.700 1.000 1 2012 2012
dbSNP: rs9939224
rs9939224
CETP
1.000 0.040 16 56968820 intron variant T/G snv 0.75
CUI: C0428472
Disease: Serum HDL cholesterol measurement
Serum HDL cholesterol measurement 		0.700 1.000 1 2012 2012