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
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
rs2395174 0.827 0.320 6 32437101 upstream gene variant T/G snv 0.24 5
rs266729 0.637 0.560 3 186841685 upstream gene variant C/A;G;T snv 37
rs361525
TNF
0.562 0.760 6 31575324 upstream gene variant G/A snv 4.6E-02 62
rs3892710 0.851 0.240 6 32715085 upstream gene variant C/T snv 0.22 4
rs9276991 0.882 0.240 6 33014071 upstream gene variant A/G snv 6.0E-02 3
rs2228570
VDR
0.521 0.760 12 47879112 start lost A/C;G;T snv 0.63 99
rs11614913 0.512 0.760 12 53991815 mature miRNA variant C/T snv 0.39 0.34 111
rs2910164 0.447 0.880 5 160485411 mature miRNA variant C/G snv 0.71; 4.1E-06 0.70 193
rs1048990 0.790 0.280 14 35292469 5 prime UTR variant C/G;T snv 0.19; 4.0E-06 8
rs143383 0.724 0.320 20 35438203 5 prime UTR variant G/A snv 0.47 17
rs12794714 0.708 0.360 11 14892029 synonymous variant G/A snv 0.41 0.35 15
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
rs1041981 0.667 0.520 6 31573007 missense variant C/A snv 0.35 0.38 25
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
rs1217691063 0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 614
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
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