Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs4734879 8 105570896 intron variant A/G snv 0.31 2
rs4541868 8 105578477 intron variant C/A snv 0.33 1
rs4602861 8 105578478 intron variant A/G;T snv 1