Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs4680 0.442 0.920 22 19963748 missense variant G/A snv 0.46 0.44 249
rs1048943 0.533 0.720 15 74720644 missense variant T/A;C;G snv 0.11 5.9E-02 88
rs1056836 0.581 0.680 2 38071060 missense variant G/C snv 0.51 58
rs1136201 0.645 0.280 17 39723335 missense variant A/G;T snv 0.20 34
rs238406 0.677 0.480 19 45365051 synonymous variant T/G snv 0.58 0.65 23
rs1469713 0.827 0.160 19 19417997 intron variant A/G snv 0.44 7
rs2066827 0.695 0.320 12 12718165 missense variant T/A;C;G snv 1.6E-04; 1.6E-05; 0.26 21
rs1695 0.457 0.880 11 67585218 missense variant A/G snv 0.34 0.36 188
rs757210 0.807 0.160 17 37736525 intron variant C/G;T snv 6
rs1899663 0.683 0.280 12 53967210 intron variant C/A snv 0.28 22
rs4759314 0.649 0.440 12 53968051 non coding transcript exon variant G/A snv 0.93 31
rs920778 0.633 0.480 12 53966448 intron variant G/A snv 0.57 36
rs138213197 0.701 0.240 17 48728343 missense variant C/T snv 1.8E-03 1.6E-03 24
rs5498 0.531 0.760 19 10285007 missense variant A/G snv 0.44 0.37 99
rs7937840 0.807 0.200 11 62126500 intron variant C/T snv 0.20 7
rs861539 0.519 0.680 14 103699416 missense variant G/A snv 0.29 0.30 104
rs13181 0.487 0.760 19 45351661 stop gained T/A;G snv 4.0E-06; 0.32 134
rs9375701 0.827 0.160 6 130062912 intron variant C/T snv 0.53 6
rs1800562 0.435 0.880 6 26092913 missense variant G/A snv 3.3E-02 3.8E-02 262
rs2910164 0.447 0.880 5 160485411 mature miRNA variant C/G snv 0.71; 4.1E-06 0.70 193
rs1799977 0.662 0.440 3 37012077 missense variant A/C;G;T snv 0.23 28
rs1217691063 0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 614
rs1801133 0.472 0.880 1 11796321 missense variant G/A snv 0.31 0.27 174
rs397507444 0.405 0.880 1 11794407 missense variant T/G snv 306
rs34612342 0.653 0.400 1 45332803 missense variant T/C snv 1.5E-03 1.6E-03 32