Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs864309483 0.851 0.080 3 123352464 missense variant G/A snv 9
rs1064794533 0.882 0.080 16 56336846 missense variant G/A snv 4
rs4704559 0.925 0.080 5 79517086 upstream gene variant A/G snv 0.15 4
rs2293054 0.925 0.080 12 117263909 synonymous variant A/G;T snv 0.69; 4.0E-06 2
rs387907128 0.925 0.080 16 29813850 missense variant C/T snv 4.0E-06 7.0E-06 2
rs1267306614 1.000 0.080 3 114171850 missense variant C/G snv 1
rs1345423 1.000 0.080 16 10154207 intron variant G/A;C;T snv 1
rs4911871 1.000 0.080 X 114762580 intron variant A/G snv 0.15 1
rs34778348 0.742 0.120 12 40363526 missense variant G/A snv 1.7E-03 5.8E-04 15
rs28363170 0.827 0.120 5 1393745 3 prime UTR variant -/AGTGGGGGCCCTGCATGCGTCCTGGGGTAGTACACGCTCC delins 8.1E-06 7
rs35801418 0.827 0.120 12 40321114 missense variant A/G snv 7
rs165815 0.882 0.120 22 19971950 missense variant C/T snv 0.75 0.72 5
rs752513525 0.882 0.120 19 19526257 missense variant G/A;T snv 2.4E-05 3
rs1554389088 0.807 0.160 7 44243526 missense variant G/A snv 27
rs113994152 0.790 0.160 17 75522000 missense variant G/T snv 9.0E-04 9.0E-04 11
rs1799836 0.790 0.160 X 43768752 intron variant T/A;C snv 0.43 7
rs1563945076 0.925 0.160 9 32974556 frameshift variant A/- del 4
rs393795 0.851 0.160 5 1428399 intron variant G/T snv 0.28 4
rs147484110 0.807 0.200 21 43774760 splice acceptor variant C/G snv 1.5E-04 2.7E-04 11
rs74315442 0.851 0.200 21 43774297 stop gained G/A snv 4.0E-05 2.1E-05 10
rs56984562 0.827 0.200 1 156137666 missense variant C/A;G;T snv 6
rs146539065 0.752 0.240 4 25145092 synonymous variant C/T snv 2.8E-05 4.2E-05 34
rs776969714 0.752 0.240 4 25145129 splice acceptor variant -/C delins 4.2E-05 34
rs139455627 0.851 0.240 21 44531087 stop gained G/A snv 3.2E-04 2.7E-04 14
rs1569151872 0.851 0.240 21 44509225 frameshift variant GAC/AA delins 14