Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs763059810 0.623 0.600 2 136115750 missense variant T/C snv 4.0E-06 41
rs121912664 0.630 0.320 17 7670699 missense variant C/A;G;T snv 1.2E-05 40
rs3834129 0.627 0.560 2 201232809 upstream gene variant AGTAAG/- del 0.48 38
rs3732379 0.637 0.680 3 39265765 missense variant C/T snv 0.22 0.22 38
rs11554290 0.583 0.600 1 114713908 missense variant T/A;C;G snv 38
rs1570360 0.641 0.680 6 43770093 upstream gene variant A/G snv 0.76 38
rs1444669684 0.658 0.480 9 21994285 missense variant C/A;T snv 36
rs2282679
GC
0.645 0.480 4 71742666 intron variant T/G snv 0.21 36
rs920778 0.633 0.480 12 53966448 intron variant G/A snv 0.57 36
rs1800625 0.641 0.680 6 32184665 upstream gene variant A/G snv 0.15 35
rs1057519695 0.641 0.520 1 114713907 missense variant TT/CA;CC mnv 35
rs20576 0.637 0.400 8 23200707 missense variant T/G snv 0.15 0.14 34
rs1136201 0.645 0.280 17 39723335 missense variant A/G;T snv 0.20 33
rs1800624 0.658 0.480 6 32184610 upstream gene variant A/G;T snv 33
rs121913227 0.653 0.320 7 140753336 missense variant AC/CT;TT mnv 31
rs2227983 0.658 0.520 7 55161562 missense variant G/A;C;T snv 0.29 31
rs1057519834 0.658 0.480 1 114713908 missense variant TG/CT mnv 31
rs486907 0.667 0.360 1 182585422 missense variant C/T snv 0.31 0.28 31
rs145204276 0.658 0.320 1 173868254 splice donor variant CAAGG/- delins 8.8E-02 31
rs1800734 0.653 0.400 3 36993455 5 prime UTR variant G/A snv 0.22 30
rs11549467 0.653 0.400 14 61740857 missense variant G/A snv 8.9E-03 7.0E-03 30
rs17577 0.649 0.520 20 46014472 missense variant G/A;C snv 0.16 30
rs61764370 0.662 0.320 12 25207290 3 prime UTR variant A/C snv 6.2E-02 29
rs121913254 0.658 0.440 1 114713909 stop gained G/A;C;T snv 29
rs752021744 0.689 0.440 3 138759306 missense variant T/C snv 1.2E-05 29