Disease: Lipids measurement
Source: GWASDB ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs3764261 0.732 0.280 16 56959412 upstream gene variant C/A snv 0.31 11
rs174547
FADS2 ; FADS1
0.742 0.240 11 61803311 intron variant T/C snv 0.28 10
rs651821
APOA5
0.851 0.360 11 116791863 5 prime UTR variant C/T snv 0.88 0.89 6
rs2575876
ABCA1
9 104903458 intron variant G/A snv 0.24 4
rs6065904
PLTP
1.000 0.080 20 45906012 intron variant G/A snv 0.23 4