Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1057519753 0.763 0.120 1 64846664 missense variant C/A snv 9
rs10994982 0.790 0.120 10 61950345 intron variant A/G snv 0.49 7
rs121909646 0.882 0.120 13 28018504 missense variant T/A;G snv 3
rs121913448 0.827 0.120 9 130862976 missense variant G/A snv 5
rs121913488 0.807 0.120 13 28018505 missense variant C/A;G;T snv 7
rs1339159756 0.925 0.120 9 5078395 missense variant C/G snv 2
rs147390019 0.925 0.120 13 48045720 missense variant G/A snv 2.6E-03 2.2E-03 2
rs17007695 0.851 0.120 4 141788570 intergenic variant T/C snv 7.7E-02 4
rs186364861 0.882 0.120 13 48037798 missense variant G/A snv 9.1E-04 2.4E-04 4
rs1966862 0.790 0.120 4 85766908 intron variant A/G snv 0.14 8
rs2274407 0.882 0.120 13 95206781 missense variant C/A;G;T snv 9.7E-02 0.10 4
rs3794845
MBP
0.882 0.120 18 77002561 intron variant G/C snv 0.12 3
rs387906517 0.827 0.120 9 130862919 missense variant G/A snv 6
rs408626 0.925 0.120 5 80655314 non coding transcript exon variant T/C snv 0.48 2
rs442767 0.925 0.120 5 80655677 intron variant G/T snv 0.27 2
rs4748793 0.851 0.120 10 22194082 intergenic variant A/G snv 0.18 4
rs6021191 0.851 0.120 20 51419700 intron variant A/T snv 4.9E-02 5
rs6964969 0.851 0.120 7 50405553 downstream gene variant A/G snv 0.23 4
rs7088318 0.851 0.120 10 22564019 intron variant C/A snv 0.55 4
rs78380171 0.925 0.120 3 86720838 intergenic variant A/G snv 6.6E-03 2
rs7896246 0.925 0.120 10 61964631 intron variant A/G snv 0.74 2
rs924607 0.851 0.120 5 609978 intron variant C/T snv 0.32 7
rs1057519773 0.851 0.160 9 130872901 missense variant T/A;C;G snv 4
rs121913451 0.851 0.160 9 130872903 missense variant C/A;G snv 4
rs121913459 0.672 0.160 9 130872896 missense variant C/T snv 25