Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1799782 0.474 0.800 19 43553422 missense variant G/A snv 9.5E-02 7.0E-02 151
rs1052133 0.476 0.800 3 9757089 missense variant C/G snv 0.27 0.22 147
rs2234693 0.555 0.680 6 151842200 intron variant T/C snv 0.47 77
rs4994 0.578 0.640 8 37966280 missense variant A/G snv 0.11 9.2E-02 65
rs9340799 0.583 0.680 6 151842246 intron variant A/G snv 0.32 62
rs351855 0.597 0.560 5 177093242 missense variant G/A snv 0.33 0.26 58
rs746702110 0.627 0.480 3 9756778 missense variant C/T snv 1.2E-05 2.8E-05 38
rs17782313 0.683 0.480 18 60183864 intergenic variant T/C snv 0.24 34
rs20575 0.645 0.440 8 23201811 missense variant C/G snv 0.54 0.44 29
rs693 0.708 0.440 2 21009323 synonymous variant G/A snv 0.39 0.38 24
rs1801132 0.689 0.320 6 151944387 synonymous variant G/C snv 0.73 0.80 22
rs4148323 0.701 0.440 2 233760498 missense variant G/A snv 2.2E-02 9.2E-03 22
rs8175347 0.708 0.400 2 233760234 intron variant TATA/-;TA;TATATA;TATATATA;TATATATATA;TATATATATATA delins 16
rs1042838
PGR
0.742 0.240 11 101062681 missense variant C/A;G snv 0.13; 4.0E-06 12
rs1111875 0.776 0.360 10 92703125 intergenic variant C/T snv 0.36 10
rs10146997 0.827 0.240 14 79478819 intron variant A/G snv 0.25 6