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: rs3905000
rs3905000
0.925 0.080 9 104894789 intron variant G/A snv 0.14
High density lipoprotein measurement
0.800 1.000 4 2009 2019
dbSNP: rs3905000
rs3905000
0.925 0.080 9 104894789 intron variant G/A snv 0.14
CUI: C1445957
Disease: Serum total cholesterol measurement
Serum total cholesterol measurement
0.700 1.000 1 2018 2018
dbSNP: rs3905000
rs3905000
0.925 0.080 9 104894789 intron variant G/A snv 0.14
CUI: C0524620
Disease: Metabolic Syndrome X
Metabolic Syndrome X
0.700 1.000 1 2018 2018