Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10770125 0.882 0.200 11 2147784 missense variant A/G snv 0.49 0.40 4
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
rs2457576 0.925 0.200 6 160444587 intron variant G/C snv 0.27 2
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
rs58624704
ALB
0.925 0.200 4 73410325 missense variant G/A snv 8.0E-06 3.5E-05 2
rs11651270 0.882 0.240 17 5521757 missense variant T/C snv 0.45 0.47 4
rs2234694 0.882 0.240 21 31666552 intron variant A/C snv 3.6E-02 3.4E-02 3
rs1800783 0.827 0.280 7 150992309 intron variant A/C;G;T snv 7
rs281432 0.851 0.280 19 10279982 intron variant C/G snv 0.52 12
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
rs759853 0.827 0.320 7 134459206 non coding transcript exon variant G/A snv 0.33 6
rs237025 0.672 0.360 6 149400554 missense variant G/A snv 0.55 0.57 26
rs316019 0.790 0.360 6 160249250 missense variant A/C snv 0.90 0.89 8
rs61758388 0.851 0.360 16 17470454 missense variant C/A;G snv 2.7E-02 4
rs10811661 0.724 0.400 9 22134095 intergenic variant T/C snv 0.14 22
rs2670660 0.708 0.400 17 5615686 intron variant A/G snv 0.41 15
rs4402960 0.724 0.400 3 185793899 intron variant G/T snv 0.38 21
rs713041 0.776 0.400 19 1106616 stop gained T/A;C snv 4.2E-06; 0.58 16
rs4762
AGT
0.637 0.440 1 230710231 missense variant G/A snv 0.12 0.11 35
rs16139 0.658 0.560 7 24285260 missense variant T/A;C snv 4.0E-06; 3.0E-02 36