Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2250205 20 35280121 splice region variant G/A snv 0.23 0.25 2
rs2425047 20 35283872 intron variant A/C;T snv 2
rs932562 20 35283507 intron variant T/C snv 0.23 2
rs2297789 20 35279445 intron variant A/T snv 0.24 2