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: rs2954029
rs2954029 		0.807 0.160 8 125478730 intron variant A/T snv 0.42
CUI: C0202236
Disease: Triglycerides measurement
Triglycerides measurement 		0.800 1.000 6 2009 2019
dbSNP: rs2954029
rs2954029 		0.807 0.160 8 125478730 intron variant A/T snv 0.42
CUI: C1445957
Disease: Serum total cholesterol measurement
Serum total cholesterol measurement 		0.800 1.000 4 2010 2019
dbSNP: rs2954029
rs2954029 		0.807 0.160 8 125478730 intron variant A/T snv 0.42
CUI: C0392885
Disease: High density lipoprotein measurement
High density lipoprotein measurement 		0.800 1.000 4 2010 2019
dbSNP: rs2954029
rs2954029 		0.807 0.160 8 125478730 intron variant A/T snv 0.42
CUI: C0202117
Disease: Low density lipoprotein cholesterol measurement
Low density lipoprotein cholesterol measurement 		0.800 1.000 4 2010 2019
dbSNP: rs2954029
rs2954029 		0.807 0.160 8 125478730 intron variant A/T snv 0.42
CUI: C1956346
Disease: Coronary Artery Disease
Coronary Artery Disease 		0.800 1.000 1 2013 2018
dbSNP: rs2954029
rs2954029 		0.807 0.160 8 125478730 intron variant A/T snv 0.42
CUI: C0428474
Disease: Serum LDL cholesterol measurement
Serum LDL cholesterol measurement 		0.700 1.000 4 2010 2013
dbSNP: rs2954029
rs2954029 		0.807 0.160 8 125478730 intron variant A/T snv 0.42
CUI: C0428472
Disease: Serum HDL cholesterol measurement
Serum HDL cholesterol measurement 		0.700 1.000 4 2010 2013