Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2910164 0.447 0.880 5 160485411 mature miRNA variant C/G snv 0.71; 4.1E-06 0.70 193
rs121913279 0.526 0.560 3 179234297 missense variant A/G;T snv 4.0E-06; 4.0E-06 101
rs121913386 0.807 0.120 9 21971018 missense variant G/A;T snv 7
rs1136410 0.559 0.760 1 226367601 missense variant A/G snv 0.21 0.15 70
rs121913240 0.672 0.440 12 25227342 missense variant T/A;C;G snv 24
rs112445441 0.658 0.400 12 25245347 missense variant C/A;G;T snv 32
rs121913529 0.492 0.680 12 25245350 missense variant C/A;G;T snv 4.0E-06 144
rs121913530 0.583 0.640 12 25245351 missense variant C/A;G;T snv 63
rs1800629
TNF
0.472 0.920 6 31575254 upstream gene variant G/A snv 0.12 0.14 169
rs121913409 0.708 0.400 3 41224646 missense variant C/A;G;T snv 21
rs25487 0.441 0.800 19 43551574 missense variant T/C snv 0.68 0.71 205
rs25489 0.550 0.720 19 43552260 missense variant C/G;T snv 8.5E-06; 7.1E-02 78
rs1799782 0.474 0.800 19 43553422 missense variant G/A snv 9.5E-02 7.0E-02 151
rs13181 0.487 0.760 19 45351661 stop gained T/A;G snv 4.0E-06; 0.32 134
rs1799793 0.557 0.640 19 45364001 missense variant C/A;T snv 7.1E-06; 0.29 72
rs17577 0.649 0.520 20 46014472 missense variant G/A;C snv 0.16 31
rs1544410
VDR
0.542 0.760 12 47846052 intron variant C/A;G;T snv 78
rs10735810
VDR
0.662 0.640 12 47879112 start lost A/C;G;T snv 26
rs77375493 0.458 0.760 9 5073770 missense variant G/A;T snv 3.5E-04 187
rs727503094 0.633 0.440 11 534287 missense variant GC/AG;AT;TA;TT mnv 41
rs104894230 0.564 0.600 11 534288 missense variant C/A;G;T snv 73
rs1870377
KDR
0.695 0.520 4 55106807 missense variant T/A snv 0.22 0.20 25
rs121434569 0.581 0.520 7 55181378 missense variant C/T snv 2.8E-05 5.6E-05 70
rs397517132 0.623 0.280 7 55191846 missense variant A/T snv 48
rs758272654 0.611 0.680 20 58909201 synonymous variant T/C snv 4.0E-06 7.0E-06 50