Source: GWASCAT

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: rs173539
rs173539 		0.882 0.080 16 56954132 intergenic variant C/T snv 0.33
CUI: C0392885
Disease: High density lipoprotein measurement
High density lipoprotein measurement 		0.800 1.000 5 2009 2019
dbSNP: rs173539
rs173539 		0.882 0.080 16 56954132 intergenic variant C/T snv 0.33
CUI: C0202236
Disease: Triglycerides measurement
Triglycerides measurement 		0.800 1.000 2 2011 2018
dbSNP: rs173539
rs173539 		0.882 0.080 16 56954132 intergenic variant C/T snv 0.33
CUI: C0524620
Disease: Metabolic Syndrome X
Metabolic Syndrome X 		0.800 1.000 1 2011 2011
dbSNP: rs173539
rs173539 		0.882 0.080 16 56954132 intergenic variant C/T snv 0.33
CUI: C1445957
Disease: Serum total cholesterol measurement
Serum total cholesterol measurement 		0.700 1.000 2 2018 2019
dbSNP: rs173539
rs173539 		0.882 0.080 16 56954132 intergenic variant C/T snv 0.33
CUI: C1611184
Disease: Calcification of coronary artery
Calcification of coronary artery 		0.700 1.000 1 2012 2012
dbSNP: rs173539
rs173539 		0.882 0.080 16 56954132 intergenic variant C/T snv 0.33
CUI: C0202117
Disease: Low density lipoprotein cholesterol measurement
Low density lipoprotein cholesterol measurement 		0.700 1.000 1 2018 2018