Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs25487 0.441 0.800 19 43551574 missense variant T/C snv 0.68 0.71 205
rs25489 0.550 0.720 19 43552260 missense variant C/G;T snv 8.5E-06; 7.1E-02 78
rs2736098 0.600 0.600 5 1293971 synonymous variant C/T snv 0.29 0.22 48
rs2736100 0.550 0.880 5 1286401 3 prime UTR variant C/A snv 0.52 83
rs2910164 0.447 0.880 5 160485411 mature miRNA variant C/G snv 0.71; 4.1E-06 0.70 193
rs3746444 0.514 0.760 20 34990448 mature miRNA variant A/G snv 0.20 0.19 105
rs397507444 0.405 0.880 1 11794407 missense variant T/G snv 306
rs401681 0.620 0.640 5 1321972 intron variant C/T snv 0.48 42
rs4986791 0.456 0.840 9 117713324 missense variant C/T snv 5.7E-02 4.9E-02 182
rs5443 0.532 0.760 12 6845711 synonymous variant C/T snv 0.36 0.44 106
rs861539 0.519 0.680 14 103699416 missense variant G/A snv 0.29 0.30 104
rs874945 0.732 0.240 12 53961667 upstream gene variant C/T snv 0.38 14
rs878854066 0.439 0.800 17 7676153 missense variant GG/AC mnv 213
rs9282861 0.658 0.440 16 28606193 missense variant C/T snv 31
rs953038635 0.590 0.800 6 159692720 missense variant G/A;T snv 8.0E-06 51