Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs3184504 0.572 0.600 12 111446804 missense variant T/A;C;G snv 0.67 24
rs204999 0.763 0.480 6 32142202 intergenic variant A/G snv 0.28 12
rs12663103 0.851 0.240 6 32193547 intron variant T/C snv 6.1E-02 7
rs2523535 0.851 0.200 6 31368473 intron variant A/G snv 0.32 7
rs2395174 0.827 0.320 6 32437101 upstream gene variant T/G snv 0.24 5
rs3892710 0.851 0.240 6 32715085 upstream gene variant C/T snv 0.22 4
rs3130361 0.925 0.160 6 30371787 intergenic variant A/G snv 0.81 3
rs423639 0.882 0.240 6 33019997 intergenic variant C/T snv 0.11 3
rs9276991 0.882 0.240 6 33014071 upstream gene variant A/G snv 6.0E-02 3
rs2508015 0.925 0.160 6 31042423 regulatory region variant G/A;C snv 2
rs492899 0.882 0.240 6 31965741 intron variant T/C snv 0.12 0.15 2