Disease: Serum HDL cholesterol measurement
Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2075650
TOMM40
0.662 0.360 19 44892362 intron variant A/G snv 0.13 0.13 45
rs4420638
APOC1
0.708 0.520 19 44919689 downstream gene variant A/G snv 0.18 43
rs13107325
SLC39A8
0.776 0.520 4 102267552 missense variant C/A;T snv 4.0E-06; 4.5E-02 34
rs1121980
FTO
0.807 0.240 16 53775335 intron variant G/A;C snv 18
rs2074356
HECTD4
0.763 0.280 12 112207597 intron variant G/A snv 3.8E-03 18
rs1883025
ABCA1
0.807 0.120 9 104902020 intron variant C/T snv 0.28 13
rs2278426
ANGPTL8 ; DOCK6
1.000 0.080 19 11239812 missense variant C/T snv 0.11 0.11 11
rs998584 6 43790159 downstream gene variant C/A snv 0.41 11
rs2925979
CMIP
1.000 0.080 16 81501185 intron variant T/A;C snv 10
rs13389219
COBLL1
1.000 0.080 2 164672366 intron variant C/T snv 0.47 9
rs1051921
MLXIPL
0.925 0.120 7 73593613 3 prime UTR variant G/A snv 0.15 8
rs10808546 8 125483576 intron variant C/T snv 0.39 7
rs605066 6 139508529 intron variant C/T snv 0.53 6
rs10019888 4 26061368 regulatory region variant A/G snv 0.17 3