Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs6265 0.436 0.760 11 27658369 missense variant C/T snv 0.19 0.15 5
rs4986790 0.438 0.800 9 117713024 missense variant A/G;T snv 6.1E-02; 4.0E-06 6
rs1695 0.457 0.880 11 67585218 missense variant A/G snv 0.34 0.36 1
rs2476601 0.498 0.800 1 113834946 missense variant A/G snv 0.93 0.93 34
rs1801282 0.500 0.840 3 12351626 missense variant C/G snv 0.11 8.9E-02 5
rs231775 0.504 0.720 2 203867991 missense variant A/G;T snv 0.42; 4.0E-06 1
rs1800871 0.508 0.800 1 206773289 5 prime UTR variant A/G snv 0.69 2
rs11614913 0.512 0.760 12 53991815 mature miRNA variant C/T snv 0.39 0.34 1
rs5498 0.531 0.760 19 10285007 missense variant A/G snv 0.44 0.37 2
rs16944 0.531 0.920 2 112837290 upstream gene variant A/G snv 0.57 1
rs763780 0.531 0.720 6 52236941 missense variant T/C snv 6.7E-02 6.6E-02 1
rs2070600 0.561 0.760 6 32183666 missense variant C/T snv 5.3E-02 3.6E-02 6
rs3184504 0.572 0.600 12 111446804 missense variant T/A;C;G snv 0.67 61
rs7574865 0.574 0.720 2 191099907 intron variant T/G snv 0.79 9
rs1883832 0.581 0.680 20 46118343 5 prime UTR variant T/C snv 0.75 0.80 7
rs61752717 0.583 0.840 16 3243407 missense variant T/A;C snv 2.8E-04 1
rs2066844 0.587 0.520 16 50712015 missense variant C/T snv 2.6E-02 2.9E-02 5
rs1801274 0.597 0.800 1 161509955 missense variant A/C;G snv 4.0E-06; 0.48 7
rs11209026 0.597 0.680 1 67240275 missense variant G/A snv 4.2E-02 4.6E-02 5
rs2228145 0.602 0.720 1 154454494 missense variant A/C;T snv 0.38; 1.2E-05 7
rs1143627 0.605 0.760 2 112836810 5 prime UTR variant G/A snv 0.56 1
rs2066845 0.611 0.600 16 50722629 missense variant G/C;T snv 1.1E-02; 2.2E-04 5
rs3732378 0.620 0.720 3 39265671 missense variant G/A snv 0.14 0.12 4
rs3087243 0.623 0.720 2 203874196 downstream gene variant G/A snv 0.37 7
rs10889677 0.627 0.720 1 67259437 3 prime UTR variant C/A snv 0.27 2