Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2943641 0.763 0.160 2 226229029 intergenic variant T/C snv 0.67 18
rs1267969615
ACE
0.532 0.760 17 63490960 missense variant T/C snv 4.0E-06 100
rs4862423 0.882 0.080 4 184805394 intron variant C/T snv 0.37 4
rs185847354 0.763 0.160 3 186854460 missense variant T/C snv 3.1E-04 7.0E-05 11
rs1042713 0.576 0.800 5 148826877 missense variant G/A snv 0.42 0.43 63
rs4994 0.578 0.640 8 37966280 missense variant A/G snv 0.11 9.2E-02 65
rs699
AGT
0.501 0.800 1 230710048 missense variant A/G snv 0.55 0.58 134
rs671 0.529 0.840 12 111803962 missense variant G/A snv 1.9E-02 5.8E-03 116
rs4076317 0.882 0.080 19 8364115 intron variant C/G snv 0.25 5
rs2476601 0.498 0.800 1 113834946 missense variant A/G snv 0.93 0.93 121
rs3135506 0.708 0.400 11 116791691 missense variant G/A;C snv 3.0E-05; 6.8E-02 26
rs662799 0.689 0.480 11 116792991 upstream gene variant G/A snv 0.90 33
rs759834365 0.448 0.760 11 27658456 missense variant C/T snv 1.2E-05 237
rs6265 0.436 0.760 11 27658369 missense variant C/T snv 0.19 0.15 272
rs1458766475 0.637 0.680 1 169732649 missense variant C/G;T snv 4.0E-06; 4.0E-06 41
rs5355 0.742 0.240 1 169726729 missense variant G/A snv 4.5E-02 3.3E-02 14
rs1020608562 0.807 0.160 3 46373738 missense variant T/C snv 4.0E-06 9
rs5443 0.532 0.760 12 6845711 synonymous variant C/T snv 0.36 0.44 106
rs10757274 0.701 0.320 9 22096056 intron variant A/G snv 0.41 22
rs1333049 0.614 0.520 9 22125504 intron variant G/C snv 0.41 60
rs1800777 0.724 0.280 16 56983407 missense variant G/A snv 3.7E-02 2.8E-02 17
rs1061170
CFH
0.561 0.720 1 196690107 missense variant C/T snv 0.68 0.64 72
rs4680 0.442 0.920 22 19963748 missense variant G/A snv 0.46 0.44 249
rs1298417395 0.882 0.080 1 176206716 missense variant C/T snv 1.4E-05 4
rs1205
CRP
0.602 0.680 1 159712443 3 prime UTR variant C/T snv 0.30 46