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: rs10468017
rs10468017
0.851 0.120 15 58386313 intron variant C/T snv 0.24
CUI: C0242383
Disease: Age related macular degeneration
Age related macular degeneration
0.890 0.900 2 2010 2019
dbSNP: rs10468017
rs10468017
0.851 0.120 15 58386313 intron variant C/T snv 0.24
High density lipoprotein measurement
0.800 1.000 3 2009 2019
dbSNP: rs10468017
rs10468017
0.851 0.120 15 58386313 intron variant C/T snv 0.24
CUI: C0524620
Disease: Metabolic Syndrome X
Metabolic Syndrome X
0.800 1.000 1 2011 2011
dbSNP: rs10468017
rs10468017
0.851 0.120 15 58386313 intron variant C/T snv 0.24
CUI: C0202236
Disease: Triglycerides measurement
Triglycerides measurement
0.800 1.000 1 2009 2018
dbSNP: rs10468017
rs10468017
0.851 0.120 15 58386313 intron variant C/T snv 0.24
CUI: C0202177
Disease: Phospholipid measurement
Phospholipid measurement
0.800 1.000 1 2012 2012
dbSNP: rs10468017
rs10468017
0.851 0.120 15 58386313 intron variant C/T snv 0.24
CUI: C0428472
Disease: Serum HDL cholesterol measurement
Serum HDL cholesterol measurement
0.700 1.000 3 2009 2012
dbSNP: rs10468017
rs10468017
0.851 0.120 15 58386313 intron variant C/T snv 0.24
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement
0.700 1.000 2 2012 2013
dbSNP: rs10468017
rs10468017
0.851 0.120 15 58386313 intron variant C/T snv 0.24
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease
0.700 1.000 1 2011 2011
dbSNP: rs10468017
rs10468017
0.851 0.120 15 58386313 intron variant C/T snv 0.24
CUI: C1168443
Disease: Pseudocholinesterase Measurement
Pseudocholinesterase Measurement
0.700 1.000 1 2011 2011
dbSNP: rs10468017
rs10468017
0.851 0.120 15 58386313 intron variant C/T snv 0.24
Corpuscular Hemoglobin Concentration Mean
0.700 1.000 1 2012 2012