Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1217691063 0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 614
rs1799983 0.430 0.880 7 150999023 missense variant T/A;G snv 0.75 246
rs1045642 0.456 0.840 7 87509329 synonymous variant A/G;T snv 0.50 214
rs2910164 0.447 0.880 5 160485411 mature miRNA variant C/G snv 0.71; 4.1E-06 0.70 193
rs662 0.485 0.840 7 95308134 missense variant T/C snv 0.38 0.42 157
rs1800795 0.494 0.840 7 22727026 intron variant C/G snv 0.71 140
rs1805087
MTR
0.496 0.800 1 236885200 missense variant A/G snv 0.20 0.21 135
rs699
AGT
0.501 0.800 1 230710048 missense variant A/G snv 0.55 0.58 134
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
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
rs2736100 0.550 0.880 5 1286401 3 prime UTR variant C/A snv 0.52 83
rs1800469 0.547 0.760 19 41354391 intron variant A/G snv 0.69 78
rs17576 0.557 0.760 20 46011586 missense variant A/G snv 0.39 0.36 73
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
rs1800566 0.576 0.680 16 69711242 missense variant G/A snv 0.25 0.21 59
rs2228145 0.602 0.720 1 154454494 missense variant A/C;T snv 0.38; 1.2E-05 57
rs3918242 0.602 0.680 20 46007337 upstream gene variant C/T snv 0.14 54
rs187238 0.602 0.680 11 112164265 intron variant C/A;G snv 48
rs964184 0.716 0.440 11 116778201 3 prime UTR variant G/C snv 0.82 47
rs10757278 0.620 0.520 9 22124478 intron variant A/G snv 0.40 44
rs4420638 0.708 0.520 19 44919689 downstream gene variant A/G snv 0.18 43
rs153109 0.623 0.600 16 28507775 intron variant T/C snv 0.43 37