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: rs3764261
rs3764261
0.732 0.280 16 56959412 upstream gene variant C/A snv 0.31
CUI: C0242383
Disease: Age related macular degeneration
Age related macular degeneration
0.860 1.000 2 2010 2018
dbSNP: rs3764261
rs3764261
0.732 0.280 16 56959412 upstream gene variant C/A snv 0.31
CUI: C0524620
Disease: Metabolic Syndrome X
Metabolic Syndrome X
0.830 1.000 2 2010 2018
dbSNP: rs3764261
rs3764261
0.732 0.280 16 56959412 upstream gene variant C/A snv 0.31
High density lipoprotein measurement
0.800 1.000 9 2008 2019
dbSNP: rs3764261
rs3764261
0.732 0.280 16 56959412 upstream gene variant C/A snv 0.31
CUI: C0202236
Disease: Triglycerides measurement
Triglycerides measurement
0.800 1.000 4 2009 2018
dbSNP: rs3764261
rs3764261
0.732 0.280 16 56959412 upstream gene variant C/A snv 0.31
CUI: C1445957
Disease: Serum total cholesterol measurement
Serum total cholesterol measurement
0.800 1.000 4 2010 2019
dbSNP: rs3764261
rs3764261
0.732 0.280 16 56959412 upstream gene variant C/A snv 0.31
Low density lipoprotein cholesterol measurement
0.800 1.000 3 2010 2019
dbSNP: rs3764261
rs3764261
0.732 0.280 16 56959412 upstream gene variant C/A snv 0.31
CUI: C0523744
Disease: Lipids measurement
Lipids measurement
0.800 1.000 1 2012 2012
dbSNP: rs3764261
rs3764261
0.732 0.280 16 56959412 upstream gene variant C/A snv 0.31
CUI: C0428472
Disease: Serum HDL cholesterol measurement
Serum HDL cholesterol measurement
0.700 1.000 8 2008 2013
dbSNP: rs3764261
rs3764261
0.732 0.280 16 56959412 upstream gene variant C/A snv 0.31
CUI: C0428474
Disease: Serum LDL cholesterol measurement
Serum LDL cholesterol measurement
0.700 1.000 3 2010 2013
dbSNP: rs3764261
rs3764261
0.732 0.280 16 56959412 upstream gene variant C/A snv 0.31
CUI: C1168443
Disease: Pseudocholinesterase Measurement
Pseudocholinesterase Measurement
0.700 1.000 1 2011 2011
dbSNP: rs3764261
rs3764261
0.732 0.280 16 56959412 upstream gene variant C/A snv 0.31
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease
0.700 1.000 1 2011 2011