Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs937475913 0.790 0.120 8 47936435 missense variant T/C snv 4.0E-06 7
rs12921862 0.763 0.200 16 331927 intron variant C/A snv 0.18 10
rs1805105 0.776 0.280 16 346264 synonymous variant A/G snv 0.61 0.69 11
rs2854744 0.695 0.520 7 45921476 intron variant G/T snv 0.48 20
rs17855750 0.695 0.480 16 28503907 missense variant A/C;T snv 6.4E-02; 4.0E-06 21
rs156697 0.672 0.560 10 104279427 missense variant A/G;T snv 0.35 25
rs10936599 0.637 0.600 3 169774313 synonymous variant C/T snv 0.29 0.21 32
rs153109 0.623 0.600 16 28507775 intron variant T/C snv 0.43 37
rs1805794
NBN
0.605 0.600 8 89978251 missense variant C/G snv 0.35 0.31 41
rs763059810 0.623 0.600 2 136115750 missense variant T/C snv 4.0E-06 41
rs2736098 0.600 0.600 5 1293971 synonymous variant C/T snv 0.29 0.22 48
rs758272654 0.611 0.680 20 58909201 synonymous variant T/C snv 4.0E-06 7.0E-06 50
rs3025039 0.576 0.720 6 43784799 3 prime UTR variant C/T snv 0.13 62
rs121913530 0.583 0.640 12 25245351 missense variant C/A;G;T snv 63
rs699947 0.570 0.680 6 43768652 upstream gene variant A/C;T snv 67
rs1799864 0.572 0.680 3 46357717 missense variant G/A snv 0.13 0.12 68
rs1130409 0.555 0.720 14 20456995 missense variant T/A;C;G snv 4.0E-06; 4.0E-06; 0.42 72
rs1799793 0.557 0.640 19 45364001 missense variant C/A;T snv 7.1E-06; 0.29 72
rs17576 0.557 0.760 20 46011586 missense variant A/G snv 0.39 0.36 73
rs2010963 0.542 0.840 6 43770613 5 prime UTR variant C/G snv 0.68 82
rs2736100 0.550 0.880 5 1286401 3 prime UTR variant C/A snv 0.52 83
rs1048943 0.533 0.720 15 74720644 missense variant T/A;C;G snv 0.11 5.9E-02 88
rs861539 0.519 0.680 14 103699416 missense variant G/A snv 0.29 0.30 104
rs3746444 0.514 0.760 20 34990448 mature miRNA variant A/G snv 0.20 0.19 105
rs11614913 0.512 0.760 12 53991815 mature miRNA variant C/T snv 0.39 0.34 111