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: rs1412444
rs1412444
LIPA
0.851 0.120 10 89243170 intron variant C/T snv 0.37
CUI: C1956346
Disease: Coronary Artery Disease
Coronary Artery Disease 		0.710 1.000 2 2013 2018
dbSNP: rs2246942
rs2246942
LIPA
0.925 0.040 10 89245129 intron variant A/C;G snv
CUI: C1956346
Disease: Coronary Artery Disease
Coronary Artery Disease 		0.700 1.000 2 2017 2018