Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs587781960 0.882 0.080 22 28689164 missense variant A/C;G;T snv 1.3E-05; 7.3E-05 4
rs6776706 0.851 0.080 3 25439731 intron variant T/A snv 0.27 4
rs749098599 0.882 0.080 1 3683085 missense variant C/T snv 4.0E-06 7.0E-06 4
rs780294601 0.851 0.080 3 12416967 missense variant G/C snv 4.4E-05 1.4E-05 4
rs781734330 0.851 0.080 1 16995981 missense variant C/T snv 4
rs10055201 0.882 0.080 5 55865274 intron variant A/G snv 0.76 3
rs1027702 0.882 0.080 1 161743067 intergenic variant C/T snv 0.51 3
rs10840002 0.882 0.080 11 8221479 downstream gene variant A/G snv 0.49 3
rs110420 0.882 0.080 11 8231502 intron variant T/C snv 0.42 3
rs11247957 0.882 0.080 1 26429683 3 prime UTR variant G/A snv 0.21 3
rs1211164799 0.882 0.080 17 49973938 missense variant A/T snv 3
rs12442054 0.882 0.080 15 74165683 intron variant G/A snv 0.12 3
rs1273925499 0.882 0.080 17 45991557 missense variant C/G;T snv 4.0E-06 3
rs1301478248 0.882 0.080 1 15495395 missense variant C/T snv 3
rs13034994 0.882 0.080 2 15938513 non coding transcript exon variant A/C;G snv 3
rs138085133 0.882 0.080 1 26022729 missense variant C/G;T snv 8.4E-04; 4.0E-06 3
rs1415224147 0.882 0.080 9 125585715 missense variant T/C snv 3
rs143864187 0.882 0.080 11 104949666 missense variant C/A snv 3
rs1442511697 0.882 0.080 2 96115494 missense variant T/C snv 7.0E-06 3
rs145976111 0.882 0.080 17 75742728 missense variant C/T snv 2.9E-03 2.3E-03 3
rs147480547 0.882 0.080 17 75740047 missense variant G/A;T snv 1.1E-03; 4.0E-06 3
rs147992979 0.882 0.080 15 88184270 missense variant G/A snv 8.0E-05 4.4E-05 3
rs17065417 0.882 0.080 6 104958399 intron variant A/C snv 0.10 3
rs17487792 0.882 0.080 2 214778776 intron variant C/T snv 0.16 3
rs17489363 0.882 0.080 2 214809617 5 prime UTR variant A/G snv 0.73 0.74 3