Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1217691063 0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 614
rs1800872 0.495 0.840 1 206773062 5 prime UTR variant T/G snv 0.69 119
rs1800896 0.507 0.800 1 206773552 intron variant T/C snv 0.41 113
rs1800871 0.508 0.800 1 206773289 5 prime UTR variant A/G snv 0.69 108
rs145204276 0.658 0.320 1 173868254 splice donor variant CAAGG/- delins 8.8E-02 31
rs1057519902 0.742 0.160 1 226064451 missense variant G/C snv 16
rs1553260624 0.763 0.080 1 226064454 missense variant G/A snv 14
rs1215600806 0.851 0.120 1 21564100 missense variant T/C snv 1.2E-05 4
rs1416572796 0.851 0.120 1 21568170 missense variant G/T snv 4.0E-06 4
rs143358506 0.851 0.120 1 21560674 missense variant T/C snv 8.0E-06 7.0E-06 4
rs59267781 0.851 0.120 1 156138657 missense variant C/G snv 4
rs231775 0.504 0.720 2 203867991 missense variant A/G;T snv 0.42; 4.0E-06 115
rs121913499 0.605 0.520 2 208248389 missense variant G/A;C;T snv 51
rs3087243 0.623 0.720 2 203874196 downstream gene variant G/A snv 0.37 44
rs5742909 0.614 0.680 2 203867624 upstream gene variant C/T snv 6.7E-02 40
rs4553808 0.672 0.320 2 203866282 upstream gene variant A/G;T snv 0.16 28
rs1872328 0.827 0.120 2 54168122 intron variant G/A snv 7.3E-02 6
rs3821204 0.807 0.160 2 102343821 3 prime UTR variant C/G snv 0.21 6
rs886041906 0.882 0.200 2 203868002 stop gained G/A snv 6
rs2372536 0.827 0.160 2 215325297 missense variant C/G snv 0.33 0.25 5
rs4150441 0.882 0.040 2 127283339 intron variant T/C snv 0.37 5
rs4150506 0.851 0.120 2 127262970 intron variant G/A snv 0.18 4
rs10208273 0.882 0.040 2 6383862 intergenic variant A/G snv 0.30 3
rs231755 0.882 0.040 2 203888846 regulatory region variant G/C snv 0.11 3
rs7591996 0.882 0.040 2 6321289 intron variant A/C snv 0.57 3