Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10496035 1.000 0.040 2 54950168 intron variant T/C;G snv 1
rs13394146 1.000 0.040 2 54948975 intron variant C/T snv 0.36 0.41 1
rs4625954 1.000 0.040 2 54948408 intron variant C/A snv 0.42 1