Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2383207 0.695 0.280 9 22115960 intron variant A/G snv 0.64 7
rs6475606 0.882 0.080 9 22081851 intron variant C/T snv 0.62 5
rs10757278 0.620 0.520 9 22124478 intron variant A/G snv 0.40 4
rs1333040 0.732 0.280 9 22083405 intron variant C/G;T snv 4
rs10757272 0.851 0.160 9 22088261 intron variant C/T snv 0.41 3
rs496892 0.827 0.160 9 22024352 intron variant C/T snv 0.40 3
rs10733376 1.000 0.080 9 22114470 intron variant G/C snv 0.64 2