Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs6475606 0.882 0.080 9 22081851 intron variant C/T snv 0.62 5
rs944797 0.882 0.120 9 22115287 intron variant T/C;G snv 0.49 5
rs1333046 0.925 0.080 9 22124124 intron variant T/A snv 0.43 4
rs10738609 1.000 0.040 9 22114496 intron variant A/C;G;T snv 3
rs10757279 0.925 0.040 9 22124631 intron variant A/G snv 0.40 3
rs2383205 0.925 0.080 9 22060936 intron variant A/C;G snv 3
rs10217586 1.000 0.040 9 22121350 intron variant A/T snv 0.52 2
rs10738606 1.000 0.040 9 22088091 intron variant A/T snv 0.42 2
rs10757277 1.000 0.040 9 22124451 intron variant A/G snv 0.40 2
rs1537376 1.000 0.040 9 22116221 intron variant T/C snv 0.49 2