Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2236947 0.882 0.040 3 50334001 intron variant C/A snv 0.39 3
rs235764 0.882 0.040 20 6773599 intron variant G/A snv 0.31 3
rs3787547 0.882 0.040 20 54067899 intron variant G/A snv 0.36 3
rs454006 0.882 0.040 19 53886867 intron variant T/C snv 0.36 3
rs7591996 0.882 0.040 2 6321289 intron variant A/C snv 0.57 3
rs9866361 0.882 0.040 3 179190061 intron variant G/A snv 0.24 3
rs998074 0.882 0.040 6 160047351 intron variant T/A;C snv 0.53 3
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
rs8103992 0.882 0.040 19 19554834 regulatory region variant A/C;T snv 3
rs13181 0.487 0.760 19 45351661 stop gained T/A;G snv 4.0E-06; 0.32 134
rs3212986 0.620 0.400 19 45409478 stop gained C/A;G;T snv 0.29; 4.3E-06; 4.3E-06 42
rs1217691063 0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 614
rs1042522 0.426 0.800 17 7676154 missense variant G/C;T snv 0.67 242
rs878854066 0.439 0.800 17 7676153 missense variant GG/AC mnv 213
rs1695 0.457 0.880 11 67585218 missense variant A/G snv 0.34 0.36 188
rs1799782 0.474 0.800 19 43553422 missense variant G/A snv 9.5E-02 7.0E-02 151
rs231775 0.504 0.720 2 203867991 missense variant A/G;T snv 0.42; 4.0E-06 115
rs1800470 0.515 0.840 19 41353016 missense variant G/A;C snv 0.55; 2.4E-04 107
rs861539 0.519 0.680 14 103699416 missense variant G/A snv 0.29 0.30 104
rs121913279 0.526 0.560 3 179234297 missense variant A/G;T snv 4.0E-06; 4.0E-06 101
rs1353702185 0.550 0.720 12 68839311 missense variant C/G snv 4.0E-06 79
rs25489 0.550 0.720 19 43552260 missense variant C/G;T snv 8.5E-06; 7.1E-02 78
rs28934576 0.554 0.600 17 7673802 missense variant C/A;G;T snv 4.0E-06; 1.6E-05 78
rs1799793 0.557 0.640 19 45364001 missense variant C/A;T snv 7.1E-06; 0.29 72