rs12678919, None

N. diseases: 10
Source: ALL
Disease N. SNPs d DSI v DPI v Chr Position Consequence Alleles Class AFEXOME AFGENOME Score vda EI vda N. PMIDs First Ref. Last Ref.
Triglycerides measurement
CUI: C0202236
Disease: Triglycerides measurement
1418 0.882 0.080 8 19986711 intergenic variant A/G snv 1.0E-01 0.800 1.000 13 2009 2019
High density lipoprotein measurement
1440 0.882 0.080 8 19986711 intergenic variant A/G snv 1.0E-01 0.800 1.000 12 2009 2019
Serum HDL cholesterol measurement
CUI: C0428472
Disease: Serum HDL cholesterol measurement
679 0.882 0.080 8 19986711 intergenic variant A/G snv 1.0E-01 0.700 1.000 5 2009 2013
Age related macular degeneration
CUI: C0242383
Disease: Age related macular degeneration
663 0.882 0.080 8 19986711 intergenic variant A/G snv 1.0E-01 0.040 0.750 4 2014 2019
Polypoidal choroidal vasculopathy
CUI: C1504336
Disease: Polypoidal choroidal vasculopathy
67 0.882 0.080 8 19986711 intergenic variant A/G snv 1.0E-01 0.020 2 2013 2015
Calcification of coronary artery
CUI: C1611184
Disease: Calcification of coronary artery
205 0.882 0.080 8 19986711 intergenic variant A/G snv 1.0E-01 0.700 1.000 1 2012 2012
Coronary heart disease
CUI: C0010068
Disease: Coronary heart disease
1178 0.882 0.080 8 19986711 intergenic variant A/G snv 1.0E-01 0.700 1.000 1 2011 2011
Pseudocholinesterase Measurement
CUI: C1168443
Disease: Pseudocholinesterase Measurement
568 0.882 0.080 8 19986711 intergenic variant A/G snv 1.0E-01 0.700 1.000 1 2011 2011
Serum albumin measurement
CUI: C0523465
Disease: Serum albumin measurement
3282 0.882 0.080 8 19986711 intergenic variant A/G snv 1.0E-01 0.700 1.000 1 2012 2012
Serum total cholesterol measurement
CUI: C1445957
Disease: Serum total cholesterol measurement
1243 0.882 0.080 8 19986711 intergenic variant A/G snv 1.0E-01 0.700 1.000 1 2013 2013