Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1883832 0.581 0.680 20 46118343 5 prime UTR variant T/C snv 0.75 0.80 52
rs1143634 0.597 0.680 2 112832813 synonymous variant G/A snv 0.19 0.19 52
rs953038635 0.590 0.800 6 159692720 missense variant G/A;T snv 8.0E-06 51
rs1143627 0.605 0.760 2 112836810 5 prime UTR variant G/A snv 0.56 47
rs1205
CRP
0.602 0.680 1 159712443 3 prime UTR variant C/T snv 0.30 46
rs2066845 0.611 0.600 16 50722629 missense variant G/C;T snv 1.1E-02; 2.2E-04 46
rs3804099 0.627 0.680 4 153703504 synonymous variant T/C snv 0.40 0.48 40
rs1800625 0.641 0.680 6 32184665 upstream gene variant A/G snv 0.15 39
rs2569190 0.620 0.560 5 140633331 intron variant A/G snv 0.57 39
rs187084 0.641 0.480 3 52227015 intron variant A/G snv 0.38 36
rs909253 0.641 0.600 6 31572536 intron variant A/G;T snv 34
rs1800624 0.658 0.480 6 32184610 upstream gene variant A/G;T snv 33
rs4919510 0.641 0.520 10 100975021 mature miRNA variant C/G snv 0.27 0.27 32
rs121917864 0.645 0.520 4 153704936 missense variant C/T snv 8.8E-05 9.8E-05 31
rs421016
GBA
0.683 0.440 1 155235252 missense variant A/C;G snv 8.0E-06; 1.3E-03 30
rs2297518 0.658 0.480 17 27769571 missense variant G/A snv 0.18 0.17 30
rs11536889 0.658 0.560 9 117715853 3 prime UTR variant G/C snv 0.11 27
rs1800450 0.662 0.640 10 52771475 missense variant C/T snv 0.14 0.11 26
rs57095329 0.677 0.480 5 160467840 intron variant A/G snv 7.8E-02 25
rs2249825 0.695 0.440 13 30463766 5 prime UTR variant G/A;C;T snv 23
rs8177374 0.672 0.520 11 126292948 missense variant C/T snv 0.12 0.11 22
rs2227306 0.677 0.680 4 73741338 intron variant C/T snv 0.31 21
rs1065489
CFH
0.695 0.440 1 196740644 missense variant G/T snv 0.20 0.15 19
rs1043210477 0.701 0.520 3 49358250 missense variant G/A snv 19
rs1045411 0.708 0.360 13 30459095 3 prime UTR variant C/T snv 0.20 18