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
rs1799945 0.452 0.760 6 26090951 missense variant C/G;T snv 0.11 0.10 226
rs699
AGT
0.501 0.800 1 230710048 missense variant A/G snv 0.55 0.58 134
rs1801282 0.500 0.840 3 12351626 missense variant C/G snv 0.11 8.9E-02 131
rs1805192 0.510 0.840 3 12379739 missense variant C/G snv 121
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
rs3746444 0.514 0.760 20 34990448 mature miRNA variant A/G snv 0.20 0.19 105
rs1267969615
ACE
0.532 0.760 17 63490960 missense variant T/C snv 4.0E-06 100
rs1137101 0.554 0.760 1 65592830 missense variant A/G snv 0.51 0.50 77
rs1042713 0.576 0.800 5 148826877 missense variant G/A snv 0.42 0.43 63
rs10757278 0.620 0.520 9 22124478 intron variant A/G snv 0.40 44
rs5370 0.630 0.520 6 12296022 missense variant G/T snv 0.23 0.21 37
rs76992529
TTR
0.653 0.560 18 31598655 missense variant G/A snv 1.1E-03 4.9E-03 36
rs1800206 0.641 0.640 22 46218377 missense variant C/G snv 4.3E-02 4.2E-02 35
rs10455872
LPA
0.662 0.320 6 160589086 intron variant A/G snv 4.3E-02 33
rs1799895 0.683 0.360 4 24800212 missense variant C/G snv 2.3E-02 1.2E-02 26
rs10757274 0.701 0.320 9 22096056 intron variant A/G snv 0.41 22
rs1022113606 0.732 0.280 4 24800161 missense variant G/C snv 1.6E-04 2.1E-05 17
rs3798220
LPA
0.732 0.160 6 160540105 missense variant T/C snv 5.6E-02 3.1E-02 16
rs12564445 0.851 0.040 1 201376359 intron variant G/A snv 0.27 5