Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10741657 0.637 0.520 11 14893332 upstream gene variant A/G snv 0.65 34
rs17300539 0.752 0.320 3 186841671 upstream gene variant G/A snv 5.3E-02 11
rs1800587 0.620 0.720 2 112785383 upstream gene variant G/A;C snv 0.32 43
rs1800629
TNF
0.472 0.920 6 31575254 upstream gene variant G/A snv 0.12 0.14 169
rs2243250
IL4
0.570 0.760 5 132673462 upstream gene variant C/T snv 0.35 61
rs266729 0.637 0.560 3 186841685 upstream gene variant C/A;G;T snv 37
rs2228570
VDR
0.521 0.760 12 47879112 start lost A/C;G;T snv 0.63 99
rs2910164 0.447 0.880 5 160485411 mature miRNA variant C/G snv 0.71; 4.1E-06 0.70 193
rs5443 0.532 0.760 12 6845711 synonymous variant C/T snv 0.36 0.44 106
rs1800796 0.555 0.760 7 22726627 non coding transcript exon variant G/C snv 9.9E-02 74
rs1042713 0.576 0.800 5 148826877 missense variant G/A snv 0.42 0.43 63
rs1063856
VWF
0.763 0.400 12 6044368 missense variant T/C;G snv 0.31 14
rs1131498 0.732 0.360 1 169707345 missense variant A/G snv 0.21 0.22 13
rs11547328 0.701 0.360 12 57751648 missense variant G/A;T snv 4.0E-06 27
rs1217691063 0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 614
rs121908261 0.851 0.120 11 2160809 missense variant G/A snv 5
rs1258159645 0.630 0.600 16 69711128 missense variant G/A snv 7.0E-06 37
rs1260326 0.645 0.600 2 27508073 missense variant T/C;G snv 0.63; 4.0E-06 0.68 81
rs1267969615
ACE
0.532 0.760 17 63490960 missense variant T/C snv 4.0E-06 100
rs13266634 0.724 0.480 8 117172544 missense variant C/A;T snv 0.29 23
rs1332629192
ALB
0.851 0.200 4 73404374 missense variant C/T snv 7
rs1416580204
MOK
0.608 0.720 14 102250837 missense variant C/T snv 4.0E-06 7.0E-06 49
rs16139 0.658 0.560 7 24285260 missense variant T/A;C snv 4.0E-06; 3.0E-02 36
rs1799983 0.430 0.880 7 150999023 missense variant T/A;G snv 0.75 246
rs1800566 0.576 0.680 16 69711242 missense variant G/A snv 0.25 0.21 59