Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs629301 0.851 0.120 1 109275684 3 prime UTR variant G/T snv 0.74 19
rs646776 0.752 0.240 1 109275908 downstream gene variant C/T snv 0.74 10
rs12740374 0.851 0.040 1 109274968 3 prime UTR variant G/T snv 0.22 9
rs7528419 0.851 0.080 1 109274570 3 prime UTR variant A/G snv 0.23 9
rs11591147 0.677 0.360 1 55039974 missense variant G/A;T snv 1.2E-02 6
rs12748152 1.000 0.120 1 26811902 upstream gene variant C/T snv 5.7E-02 6
rs2642438 1 220796686 missense variant A/G snv 0.75 0.78 6
rs599839 0.724 0.360 1 109279544 downstream gene variant G/A;C snv 6
rs114165349 1 26695422 intron variant G/C snv 1.7E-02 5
rs79598313 1 26958422 intron variant C/A;T snv 5
rs10889353 1 62652525 intron variant A/C;T snv 4
rs10900522 1 205714939 3 prime UTR variant T/C snv 0.21 4
rs11206510 0.763 0.240 1 55030366 intergenic variant T/A;C;G snv 4
rs1167998 1 62465961 intron variant C/A snv 0.57 4
rs1748195 0.851 0.120 1 62583922 intron variant C/G;T snv 4
rs3761959 0.827 0.320 1 157699488 intron variant C/A;G;T snv 4
rs4495740 1 62658794 intron variant T/G snv 0.34 4
rs586178 1 25420739 missense variant G/A;C snv 8.4E-05; 0.41 4
rs10889348 1 62612551 intron variant A/T snv 0.32 3
rs10903129 1 25442446 intron variant A/G snv 0.58 3
rs11207995 1 62583880 intron variant A/C;G snv 3
rs1168013 1.000 0.120 1 62531167 intron variant C/G;T snv 3
rs12042319 1.000 0.040 1 62584148 3 prime UTR variant G/A snv 0.36 3
rs12047226 1 62639867 intron variant T/A;C snv 3
rs1689788 1 182175287 intron variant T/C snv 0.29 3