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: rs2083637
rs2083637 		0.925 0.080 8 20007664 intergenic variant A/G snv 0.25
CUI: C0392885
Disease: High density lipoprotein measurement
High density lipoprotein measurement 		0.800 1.000 2 2009 2019
dbSNP: rs2083637
rs2083637 		0.925 0.080 8 20007664 intergenic variant A/G snv 0.25
CUI: C0202236
Disease: Triglycerides measurement
Triglycerides measurement 		0.800 1.000 1 2012 2019
dbSNP: rs2083637
rs2083637 		0.925 0.080 8 20007664 intergenic variant A/G snv 0.25
CUI: C0524620
Disease: Metabolic Syndrome X
Metabolic Syndrome X 		0.800 1.000 1 2010 2010
dbSNP: rs2083637
rs2083637 		0.925 0.080 8 20007664 intergenic variant A/G snv 0.25
CUI: C0428472
Disease: Serum HDL cholesterol measurement
Serum HDL cholesterol measurement 		0.700 1.000 2 2009 2012
dbSNP: rs2083637
rs2083637 		0.925 0.080 8 20007664 intergenic variant A/G snv 0.25
CUI: C1168443
Disease: Pseudocholinesterase Measurement
Pseudocholinesterase Measurement 		0.700 1.000 1 2011 2011
dbSNP: rs2083637
rs2083637 		0.925 0.080 8 20007664 intergenic variant A/G snv 0.25
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease 		0.700 1.000 1 2011 2011