Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs9579646 0.851 0.160 13 30736442 intron variant G/A;T snv 6
rs899127658
F2
0.547 0.720 11 46739084 missense variant G/A;C snv 82
rs886205 0.827 0.360 12 111766623 intron variant A/G snv 0.35 8
rs854560 0.513 0.800 7 95316772 missense variant A/C;G;N;T snv 0.29 113
rs822396 0.732 0.400 3 186849088 intron variant G/A snv 0.81 16
rs8192284 0.724 0.720 1 154454494 missense variant A/C;T snv 19
rs7950273 0.925 0.120 11 104160870 intron variant C/G snv 0.32 5
rs7903146 0.554 0.680 10 112998590 intron variant C/G;T snv 93
rs76863441 0.672 0.440 6 46709361 missense variant C/A snv 4.5E-03 1.3E-03 25
rs759834365 0.448 0.760 11 27658456 missense variant C/T snv 1.2E-05 237
rs751377893
F5
0.574 0.680 1 169546513 missense variant T/C snv 4.0E-06 65
rs7493 0.677 0.440 7 95405463 missense variant G/C snv 0.27 0.27 24
rs746682028 0.645 0.480 11 27658414 missense variant C/A;T snv 4.0E-06; 4.0E-06 36
rs7193788 0.925 0.120 16 82622555 upstream gene variant A/G snv 0.16 4
rs699
AGT
0.501 0.800 1 230710048 missense variant A/G snv 0.55 0.58 134
rs662799 0.689 0.480 11 116792991 upstream gene variant G/A snv 0.90 33
rs662 0.485 0.840 7 95308134 missense variant T/C snv 0.38 0.42 157
rs6265 0.436 0.760 11 27658369 missense variant C/T snv 0.19 0.15 272
rs5443 0.532 0.760 12 6845711 synonymous variant C/T snv 0.36 0.44 106
rs5361 0.623 0.720 1 169731919 missense variant T/G snv 8.3E-02; 8.0E-06 7.8E-02 47
rs5355 0.742 0.240 1 169726729 missense variant G/A snv 4.5E-02 3.3E-02 14
rs5275 0.583 0.560 1 186673926 3 prime UTR variant A/G;T snv 55
rs5186 0.630 0.560 3 148742201 3 prime UTR variant A/C snv 0.23 0.21 38
rs505151 0.732 0.360 1 55063514 missense variant G/A snv 0.95 0.90 18
rs4986791 0.456 0.840 9 117713324 missense variant C/T snv 5.7E-02 4.9E-02 182