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: rs2169387
rs2169387
LOC157273
8 9323885 intron variant A/G snv 0.87
CUI: C0202117
Disease: Low density lipoprotein cholesterol measurement
Low density lipoprotein cholesterol measurement 		0.700 1.000 3 2015 2018
dbSNP: rs2169387
rs2169387
LOC157273
8 9323885 intron variant A/G snv 0.87
CUI: C1445957
Disease: Serum total cholesterol measurement
Serum total cholesterol measurement 		0.700 1.000 3 2018 2019
dbSNP: rs2169387
rs2169387
LOC157273
8 9323885 intron variant A/G snv 0.87
CUI: C0392885
Disease: High density lipoprotein measurement
High density lipoprotein measurement 		0.700 1.000 2 2018 2019
dbSNP: rs2169387
rs2169387
LOC157273
8 9323885 intron variant A/G snv 0.87
CUI: C0202236
Disease: Triglycerides measurement
Triglycerides measurement 		0.700 1.000 1 2018 2018
dbSNP: rs2169387
rs2169387
LOC157273
8 9323885 intron variant A/G snv 0.87
CUI: C0202202
Disease: Protein measurement
Protein measurement 		0.700 1.000 1 2016 2016
dbSNP: rs2169387
rs2169387
LOC157273
8 9323885 intron variant A/G snv 0.87
CUI: C0201874
Disease: Amino acids measurement
Amino acids measurement 		0.700 1.000 1 2016 2016