Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs3742330 0.662 0.640 14 95087025 3 prime UTR variant A/G snv 8.7E-02 24
rs3757441 0.752 0.200 7 148827660 intron variant C/T snv 0.80 12
rs3783553 0.667 0.480 2 112774138 3 prime UTR variant -/TGAA delins 26
rs3834129 0.627 0.560 2 201232809 upstream gene variant AGTAAG/- del 0.48 38
rs397507444 0.405 0.880 1 11794407 missense variant T/G snv 306
rs4135385 0.742 0.320 3 41237949 non coding transcript exon variant A/G snv 0.19 14
rs4444903
EGF
0.630 0.360 4 109912954 5 prime UTR variant A/G snv 0.51 35
rs4675379 0.851 0.120 2 203961372 3 prime UTR variant G/C snv 0.15 4
rs4938723 0.574 0.680 11 111511840 intron variant T/C snv 0.32 60
rs4950928 0.653 0.560 1 203186754 upstream gene variant G/A;C;T snv 32
rs5275 0.583 0.560 1 186673926 3 prime UTR variant A/G;T snv 55
rs6983267 0.578 0.440 8 127401060 non coding transcript exon variant G/T snv 0.37 55
rs712 0.677 0.360 12 25209618 3 prime UTR variant A/C snv 0.46 24
rs7421861 0.790 0.200 2 241853198 intron variant A/G;T snv 9
rs7763881 0.776 0.160 6 8653014 non coding transcript exon variant A/C snv 0.44 11
rs7799039 0.649 0.560 7 128238730 upstream gene variant G/A;C snv 33
rs878854066 0.439 0.800 17 7676153 missense variant GG/AC mnv 213
rs1217691063 0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 614
rs231775 0.504 0.720 2 203867991 missense variant A/G;T snv 0.42; 4.0E-06 114
rs7041
GC
0.576 0.800 4 71752617 missense variant A/C;T snv 0.52; 4.0E-06 61
rs759412116 0.581 0.640 19 45352210 missense variant C/G;T snv 4.0E-06; 6.0E-05 55
rs13181 0.487 0.760 19 45351661 stop gained T/A;G snv 4.0E-06; 0.32 134
rs750521832 0.732 0.200 11 102718452 missense variant A/G snv 4.0E-06 14
rs1353702185 0.550 0.720 12 68839311 missense variant C/G snv 4.0E-06 79
rs1130409 0.555 0.720 14 20456995 missense variant T/A;C;G snv 4.0E-06; 4.0E-06; 0.42 72