Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs11844632 0.708 0.280 14 68559662 intron variant G/A snv 0.23 17
rs12601991 0.708 0.280 17 37741642 intron variant T/A;G snv 17
rs4808075 0.701 0.280 19 17279482 intron variant T/C snv 0.26 18
rs11907546 0.708 0.280 20 34131991 upstream gene variant C/A;T snv 17
rs2300206 0.708 0.280 20 34002002 intron variant G/C;T snv 17