Disease: Low density lipoprotein cholesterol measurement
Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs247616 1.000 0.040 16 56955678 intergenic variant C/T snv 0.29 8
rs247617 0.827 0.160 16 56956804 regulatory region variant C/A snv 0.29 20
rs2523575 6 31361049 upstream gene variant C/G snv 0.20 4
rs2954021 1.000 0.040 8 125469835 intron variant A/G snv 0.54 15
rs2954022 8 125470379 intron variant C/A;T snv 4
rs2954029 0.807 0.160 8 125478730 intron variant A/T snv 0.42 14
rs2954031 8 125479491 intron variant G/T snv 0.42 9
rs2965101 1.000 0.080 19 44734556 intergenic variant T/C snv 0.34 6
rs2980869 8 125476008 intron variant C/T snv 0.48 6
rs2980875 8 125469505 intron variant A/C;G;T snv 6
rs2980880 8 125468730 intron variant G/A snv 0.69 6
rs3764261 0.732 0.280 16 56959412 upstream gene variant C/A snv 0.31 26
rs4360309 8 125511281 intron variant C/G;T snv 3
rs4418728 10 93079967 downstream gene variant G/T snv 0.42 8
rs4564803 2 20982630 intergenic variant G/T snv 0.25 5
rs4665710 2 20998163 downstream gene variant A/C snv 0.76 6
rs478442 0.851 0.120 2 21176344 intergenic variant G/C;T snv 18
rs4850047 2 3587163 regulatory region variant T/C snv 0.84 4
rs495828 0.827 0.200 9 133279294 upstream gene variant T/G snv 0.81 24
rs5014650 6 160678471 upstream gene variant G/A snv 0.16 4
rs506585 2 21174310 intergenic variant G/A;C;T snv 4
rs509728 11 116662450 downstream gene variant G/C snv 2.7E-02 5
rs541041 2 21072103 intergenic variant G/A snv 0.71 3
rs56156922 16 56953457 intergenic variant T/C snv 0.26 5
rs562338 0.807 0.160 2 21065449 intergenic variant A/G snv 0.69 21