Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1800562 0.435 0.880 6 26092913 missense variant G/A snv 3.3E-02 3.8E-02 34
rs1799945 0.452 0.760 6 26090951 missense variant C/G;T snv 0.11 0.10 31
rs671 0.529 0.840 12 111803962 missense variant G/A snv 1.9E-02 5.8E-03 29
rs28929474 0.708 0.320 14 94378610 missense variant C/G;T snv 2.8E-05; 1.1E-02 23
rs757075712 0.763 0.200 10 58390856 missense variant C/T snv 1.6E-05 1.4E-05 14
rs77375493 0.458 0.760 9 5073770 missense variant G/A;T snv 3.5E-04 13
rs738409 0.557 0.720 22 43928847 missense variant C/G snv 0.28 0.22 13
rs7574865 0.574 0.720 2 191099907 intron variant T/G snv 0.79 11
rs2896019 0.790 0.160 22 43937814 intron variant T/G snv 0.20 10
rs1553553086 0.827 0.280 2 222623699 missense variant C/T snv 9
rs12075 0.724 0.240 1 159205564 missense variant G/A snv 0.51 0.66 8
rs2066844 0.587 0.520 16 50712015 missense variant C/T snv 2.6E-02 2.9E-02 8
rs17580 0.776 0.160 14 94380925 missense variant T/A snv 2.3E-02 2.9E-02 8
rs367956522 0.851 0.240 13 51949798 splice acceptor variant T/C snv 2.4E-05 7.7E-05 7
rs4986790 0.438 0.800 9 117713024 missense variant A/G;T snv 6.1E-02; 4.0E-06 6
rs3135363 0.776 0.360 6 32421871 intergenic variant A/G snv 0.24 5
rs1396171148 0.851 0.200 2 222613892 missense variant T/G snv 5
rs1419129874 0.851 0.200 2 222642894 missense variant A/G snv 7.0E-06 5
rs1466642025 0.851 0.200 2 222631635 missense variant A/G snv 7.0E-06 5
rs1553554543 0.851 0.200 2 222631606 missense variant T/C snv 5
rs2596542 0.724 0.200 6 31398818 upstream gene variant C/T snv 0.41 5
rs58542926 0.630 0.440 19 19268740 missense variant C/T snv 6.5E-02 5.8E-02 5
rs910049 0.776 0.400 6 32347950 intron variant T/C snv 0.76 5
rs3129859 0.827 0.320 6 32433162 intergenic variant G/C;T snv 4
rs699
AGT
0.501 0.800 1 230710048 missense variant A/G snv 0.55 0.58 4