Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1042522 0.426 0.800 17 7676154 missense variant G/C;T snv 0.67 242
rs1042714 0.597 0.640 5 148826910 stop gained G/C;T snv 0.68 54
rs1181860747 0.776 0.240 19 7122961 missense variant C/T snv 10
rs1188383936
F2
0.524 0.760 11 46725976 missense variant C/T snv 8.0E-06 102
rs1232898090 0.637 0.600 22 46198429 missense variant G/C;T snv 4.0E-06; 4.0E-06 40
rs1267969615
ACE
0.532 0.760 17 63490960 missense variant T/C snv 4.0E-06 100
rs1320702652 0.752 0.160 15 43824536 missense variant G/A snv 4.0E-06 11
rs13266634 0.724 0.480 8 117172544 missense variant C/A;T snv 0.29 23
rs1378942
CSK
0.790 0.240 15 74785026 intron variant C/A;T snv 16
rs142648132
MTR
0.827 0.160 1 236816521 missense variant G/A;C;T snv 8.4E-04; 2.4E-05 5
rs1501299 0.597 0.720 3 186853334 intron variant G/C;T snv 52
rs16139 0.658 0.560 7 24285260 missense variant T/A;C snv 4.0E-06; 3.0E-02 36
rs16998073 0.925 0.120 4 80263187 upstream gene variant A/G;T snv 10
rs1799883 0.658 0.440 4 119320747 missense variant T/A;C;G snv 0.73 36
rs1799983 0.430 0.880 7 150999023 missense variant T/A;G snv 0.75 246
rs1800470 0.515 0.840 19 41353016 missense variant G/A;C snv 0.55; 2.4E-04 107
rs1800588 0.790 0.200 15 58431476 intron variant C/G;T snv 0.30 16
rs1800947
CRP
0.683 0.440 1 159713648 splice region variant C/A;G;T snv 4.4E-05; 5.1E-02; 4.0E-06 28
rs1805097 0.689 0.360 13 109782884 missense variant C/G;T snv 0.35 22
rs1805192 0.510 0.840 3 12379739 missense variant C/G snv 121
rs1982073 0.649 0.640 19 41353016 missense variant G/A;C snv 32
rs2032582 0.538 0.800 7 87531302 missense variant A/C;T snv 0.54; 3.8E-02 97
rs2228145 0.602 0.720 1 154454494 missense variant A/C;T snv 0.38; 1.2E-05 57
rs2241766 0.608 0.720 3 186853103 synonymous variant T/C;G snv 8.0E-06; 0.13 48
rs2297508 0.790 0.240 17 17812003 synonymous variant C/G;T snv 0.50; 7.5E-05 8