Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1799983 0.430 0.880 7 150999023 missense variant T/A;G snv 0.75 246
rs1695 0.457 0.880 11 67585218 missense variant A/G snv 0.34 0.36 188
rs699
AGT
0.501 0.800 1 230710048 missense variant A/G snv 0.55 0.58 134
rs1801282 0.500 0.840 3 12351626 missense variant C/G snv 0.11 8.9E-02 131
rs1805192 0.510 0.840 3 12379739 missense variant C/G snv 121
rs671 0.529 0.840 12 111803962 missense variant G/A snv 1.9E-02 5.8E-03 116
rs5443 0.532 0.760 12 6845711 synonymous variant C/T snv 0.36 0.44 106
rs2275913 0.514 0.760 6 52186235 upstream gene variant G/A snv 0.28 105
rs3746444 0.514 0.760 20 34990448 mature miRNA variant A/G snv 0.20 0.19 105
rs1267969615
ACE
0.532 0.760 17 63490960 missense variant T/C snv 4.0E-06 100
rs9939609
FTO
0.559 0.720 16 53786615 intron variant T/A snv 0.41 98
rs1137101 0.554 0.760 1 65592830 missense variant A/G snv 0.51 0.50 77
rs1042713 0.576 0.800 5 148826877 missense variant G/A snv 0.42 0.43 63
rs780094 0.658 0.400 2 27518370 intron variant T/C snv 0.67 62
rs1333049 0.614 0.520 9 22125504 intron variant G/C snv 0.41 60
rs28362491 0.592 0.720 4 102500998 non coding transcript exon variant ATTG/- delins 56
rs1042714 0.597 0.640 5 148826910 stop gained G/C;T snv 0.68 54
rs2070744 0.608 0.680 7 150992991 intron variant C/T snv 0.70 54
rs964184 0.716 0.440 11 116778201 3 prime UTR variant G/C snv 0.82 47
rs4149056 0.633 0.480 12 21178615 missense variant T/C snv 0.13 0.12 45
rs4420638 0.708 0.520 19 44919689 downstream gene variant A/G snv 0.18 43
rs1800625 0.641 0.680 6 32184665 upstream gene variant A/G snv 0.15 39
rs5186 0.630 0.560 3 148742201 3 prime UTR variant A/C snv 0.23 0.21 38
rs5370 0.630 0.520 6 12296022 missense variant G/T snv 0.23 0.21 37
rs76992529
TTR
0.653 0.560 18 31598655 missense variant G/A snv 1.1E-03 4.9E-03 36