Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2075650 0.662 0.360 19 44892362 intron variant A/G snv 0.13 0.13 20
rs11136000
CLU
0.752 0.160 8 27607002 intron variant T/C snv 0.56 3
rs3851179 0.752 0.280 11 86157598 downstream gene variant T/C snv 0.70 3
rs11767557 0.882 0.080 7 143412046 intron variant T/C snv 0.18 2
rs3764650 0.790 0.200 19 1046521 intron variant T/G snv 0.14 2
rs3865444 0.851 0.160 19 51224706 upstream gene variant C/A snv 0.25 2
rs610932 0.851 0.080 11 60171834 downstream gene variant T/G snv 0.57 2
rs744373 0.851 0.160 2 127137039 downstream gene variant A/G snv 0.35 2
rs9349407 1.000 0.080 6 47485642 intron variant G/C snv 0.23 2