Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2622629 0.882 0.160 4 88172912 intron variant T/C snv 0.28 2
rs1481014 0.882 0.160 4 88175999 intron variant C/A;T snv 0.24 1
rs1481017 0.882 0.160 4 88176325 intron variant C/T snv 0.59 1
rs2127863 0.882 0.160 4 88190316 intron variant T/C snv 0.84 1
rs7658584 1.000 0.040 4 88175489 intron variant G/A snv 0.24 1
rs7682521 1.000 0.040 4 88175275 intron variant T/G snv 0.24 1