Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1260326 0.645 0.600 2 27508073 missense variant T/C;G snv 0.63; 4.0E-06 0.68 55
rs780094 0.658 0.400 2 27518370 intron variant T/C snv 0.67 35
rs780092 0.827 0.160 2 27520287 intron variant A/G snv 0.18 4
rs3817588 0.882 0.160 2 27508345 intron variant T/C snv 0.14 3
rs6547692 1.000 0.080 2 27512105 intron variant G/A snv 0.58 2