Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1550117 0.790 0.320 2 25343038 upstream gene variant A/G;T snv 11
rs1569686 0.752 0.400 20 32779273 intron variant G/A;C;T snv 15
rs10434 0.701 0.480 6 43785475 3 prime UTR variant A/G snv 0.59 17
rs4778889 0.683 0.480 15 81296654 intron variant T/C snv 0.24 24
rs1760944 0.672 0.480 14 20454990 non coding transcript exon variant T/C;G snv 26
rs11556218 0.653 0.600 15 81305928 missense variant T/G snv 9.6E-02 0.12 27
rs1143623 0.677 0.440 2 112838252 upstream gene variant C/G snv 0.24 29
rs4444903
EGF
0.630 0.360 4 109912954 5 prime UTR variant A/G snv 0.51 35
rs266729 0.637 0.560 3 186841685 upstream gene variant C/A;G;T snv 37
rs2273535 0.645 0.360 20 56386485 missense variant A/C;T snv 0.28 38
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
rs2292832 0.605 0.640 2 240456086 non coding transcript exon variant T/A;C snv 0.59 46
rs758272654 0.611 0.680 20 58909201 synonymous variant T/C snv 4.0E-06 7.0E-06 50
rs28362491 0.592 0.720 4 102500998 non coding transcript exon variant ATTG/- delins 56
rs2243250
IL4
0.570 0.760 5 132673462 upstream gene variant C/T snv 0.35 61
rs3025039 0.576 0.720 6 43784799 3 prime UTR variant C/T snv 0.13 62
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
rs1353702185 0.550 0.720 12 68839311 missense variant C/G snv 4.0E-06 79
rs731236
VDR
0.542 0.760 12 47844974 synonymous variant A/G snv 0.33 0.34 81
rs2010963 0.542 0.840 6 43770613 5 prime UTR variant C/G snv 0.68 82