rs6066394, NCOA3

N. diseases: 2
Source: ALL
Disease N. SNPs d DSI v DPI v Chr Position Consequence Alleles Class AFEXOME AFGENOME Score vda EI vda N. PMIDs First Ref. Last Ref.
Hypercholesterolemia
CUI: C0020443
Disease: Hypercholesterolemia
123 1.000 0.040 20 47581409 intron variant C/T snv 0.29 0.010 1.000 1 2015 2015
Hypertriglyceridemia
CUI: C0020557
Disease: Hypertriglyceridemia
169 1.000 0.040 20 47581409 intron variant C/T snv 0.29 0.010 1.000 1 2015 2015