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 81
rs964184 0.716 0.440 11 116778201 3 prime UTR variant G/C snv 0.82 47
rs10468017 0.851 0.120 15 58386313 intron variant C/T snv 0.24 12
rs4775041 1.000 0.040 15 58382496 intron variant G/C snv 0.24 8