Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs113488022 0.351 0.840 7 140753336 missense variant A/C;G;T snv 4.0E-06 22
rs121913377 0.354 0.840 7 140753335 missense variant CA/AT;TT mnv 2
rs1799983 0.430 0.880 7 150999023 missense variant T/A;G snv 0.75 1
rs1800562 0.435 0.880 6 26092913 missense variant G/A snv 3.3E-02 3.8E-02 34
rs6265 0.436 0.760 11 27658369 missense variant C/T snv 0.19 0.15 8
rs4986790 0.438 0.800 9 117713024 missense variant A/G;T snv 6.1E-02; 4.0E-06 6
rs1131691014 0.439 0.800 17 7676154 frameshift variant -/C ins 1
rs1799945 0.452 0.760 6 26090951 missense variant C/G;T snv 0.11 0.10 31
rs1695 0.457 0.880 11 67585218 missense variant A/G snv 0.34 0.36 1
rs77375493 0.458 0.760 9 5073770 missense variant G/A;T snv 3.5E-04 13
rs1801133 0.472 0.880 1 11796321 missense variant G/A snv 0.31 0.27 6
rs662 0.485 0.840 7 95308134 missense variant T/C snv 0.38 0.42 4
rs13181 0.487 0.760 19 45351661 stop gained T/A;G snv 4.0E-06; 0.32 1
rs121913529 0.492 0.680 12 25245350 missense variant C/A;G;T snv 4.0E-06 21
rs1800795 0.494 0.840 7 22727026 intron variant C/G snv 0.71 1
rs1800872 0.495 0.840 1 206773062 5 prime UTR variant T/G snv 0.69 1
rs1801282 0.500 0.840 3 12351626 missense variant C/G snv 0.11 8.9E-02 5
rs699
AGT
0.501 0.800 1 230710048 missense variant A/G snv 0.55 0.58 4
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
rs1805192 0.510 0.840 3 12379739 missense variant C/G snv 4
rs11614913 0.512 0.760 12 53991815 mature miRNA variant C/T snv 0.39 0.34 1
rs854560 0.513 0.800 7 95316772 missense variant A/C;G;N;T snv 0.29 3
rs1800470 0.515 0.840 19 41353016 missense variant G/A;C snv 0.55; 2.4E-04 1
rs861539 0.519 0.680 14 103699416 missense variant G/A snv 0.29 0.30 1