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: rs3905000
rs3905000
0.925 0.080 9 104894789 intron variant G/A snv 0.14
High density lipoprotein measurement
0.800 1.000 1 2009 2019
dbSNP: rs3905000
rs3905000
0.925 0.080 9 104894789 intron variant G/A snv 0.14
CUI: C0428472
Disease: Serum HDL cholesterol measurement
Serum HDL cholesterol measurement
0.700 1.000 1 2009 2009
dbSNP: rs3905000
rs3905000
0.925 0.080 9 104894789 intron variant G/A snv 0.14
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease
0.700 1.000 1 2011 2011