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: rs1874124
rs1874124
1 220801995 intron variant C/T snv 0.11
CUI: C1445957
Disease: Serum total cholesterol measurement
Serum total cholesterol measurement
0.700 1.000 2 2015 2018
dbSNP: rs1874124
rs1874124
1 220801995 intron variant C/T snv 0.11
Low density lipoprotein cholesterol measurement
0.700 1.000 1 2018 2018