Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs8024137 15 35545096 intron variant A/T snv 0.88 2
rs1989223 15 35834905 intron variant T/C snv 0.21 1
rs35000814 15 35648042 intron variant A/G;T snv 1