Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs3813034 0.827 0.160 17 30197786 3 prime UTR variant A/C snv 0.40 8
rs140701 0.790 0.200 17 30211514 intron variant C/T snv 0.40 7
rs1386494 0.790 0.120 12 71958763 intron variant T/C;G snv 0.82 7
rs4565946 0.827 0.080 12 71942989 intron variant C/A;G;T snv 7
rs3749034 0.827 0.040 2 170816965 5 prime UTR variant G/A;T snv 6
rs17689918 0.851 0.080 17 45832722 intron variant G/A snv 0.15 6
rs945032 0.882 0.040 14 96204324 upstream gene variant T/C snv 0.78 5
rs1245554802 0.851 0.120 3 9765892 splice acceptor variant T/C snv 4.0E-06 5
rs771306418 0.851 0.120 3 9765885 splice acceptor variant -/C delins 5
rs4722999 0.851 0.080 7 30654159 intron variant C/T snv 0.67 5
rs17466684 0.925 0.120 8 27595330 downstream gene variant G/A snv 0.15 5
rs1173546708 0.851 0.120 11 18040661 synonymous variant G/A snv 4.0E-06 5
rs1800857 0.851 0.120 4 26489489 splice region variant A/G snv 0.17 0.18 4
rs2296972 0.925 0.080 13 46854336 intron variant A/C snv 0.70 4
rs1133503 1.000 0.040 6 95606712 3 prime UTR variant C/G;T snv 4
rs10801153 0.925 0.080 1 192794818 intron variant G/A snv 0.27 3
rs12579350 0.882 0.080 12 5687935 intron variant G/A snv 0.12 3
rs754635
CCK
1.000 0.040 3 42263639 splice region variant C/G;T snv 0.84; 5.6E-06 3
rs242924 0.882 0.080 17 45808001 intron variant G/T snv 0.44 3
rs173365 0.882 0.080 17 45823708 intron variant A/G snv 0.55 3
rs2910931 0.925 0.080 5 32394809 intron variant T/A snv 0.63 3
rs10894993 0.925 0.080 11 100627998 intergenic variant T/G snv 4.7E-02 2
rs11210604 0.925 0.080 1 42158001 downstream gene variant T/A;G snv 2
rs7688285 0.925 0.040 4 157047466 intergenic variant G/A snv 0.10 2
rs1799923
CCK
0.925 0.040 3 42264802 5 prime UTR variant A/G snv 0.82 2