Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10811661 0.724 0.400 9 22134095 intergenic variant T/C snv 0.14 22
rs12976445 0.689 0.600 19 51693200 non coding transcript exon variant T/C snv 0.45 20
rs1326934 0.925 0.200 10 95524324 intron variant C/T snv 0.63 2
rs1332629192
ALB
0.851 0.200 4 73404374 missense variant C/T snv 7
rs1567438 0.925 0.200 6 160458599 intron variant T/C snv 0.25 3
rs17300539 0.752 0.320 3 186841671 upstream gene variant G/A snv 5.3E-02 11
rs1800764 0.790 0.320 17 63473168 upstream gene variant C/G;T snv 10
rs1800783 0.827 0.280 7 150992309 intron variant A/C;G;T snv 7
rs1800795 0.494 0.840 7 22727026 intron variant C/G snv 0.71 140
rs1800796 0.555 0.760 7 22726627 non coding transcript exon variant G/C snv 9.9E-02 74
rs1805192 0.510 0.840 3 12379739 missense variant C/G snv 121
rs2243250
IL4
0.570 0.760 5 132673462 upstream gene variant C/T snv 0.35 61
rs2457576 0.925 0.200 6 160444587 intron variant G/C snv 0.27 2
rs266729 0.637 0.560 3 186841685 upstream gene variant C/A;G;T snv 37
rs2670660 0.708 0.400 17 5615686 intron variant A/G snv 0.41 15
rs281432 0.851 0.280 19 10279982 intron variant C/G snv 0.52 12
rs3773885
MME
0.925 0.200 3 155141792 intron variant G/A snv 0.33 2
rs3796268
MME
0.925 0.200 3 155117435 intron variant T/C snv 0.30 2
rs3820589 0.925 0.200 1 42960373 intron variant A/T snv 8.3E-02 2
rs397507444 0.405 0.880 1 11794407 missense variant T/G snv 306
rs4402960 0.724 0.400 3 185793899 intron variant G/T snv 0.38 21
rs759853 0.827 0.320 7 134459206 non coding transcript exon variant G/A snv 0.33 6
rs7903146 0.554 0.680 10 112998590 intron variant C/G;T snv 93
rs1217691063 0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 614
rs1267969615
ACE
0.532 0.760 17 63490960 missense variant T/C snv 4.0E-06 100