Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs17271340 15 62055686 intron variant C/T snv 0.33 2
rs2042608 15 61940181 intron variant C/A snv 0.48 2
rs17271305 15 62040781 intron variant A/G;T snv 1