Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1217691063 0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 614
rs25487 0.441 0.800 19 43551574 missense variant T/C snv 0.68 0.71 205
rs1800795 0.494 0.840 7 22727026 intron variant C/G snv 0.71 140
rs8192284 0.724 0.720 1 154454494 missense variant A/C;T snv 19
rs2834167 0.752 0.360 21 33268483 missense variant A/G snv 0.33 0.25 11