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
rs2476601 0.498 0.800 1 113834946 missense variant A/G snv 0.93 0.93 121
rs7574865 0.574 0.720 2 191099907 intron variant T/G snv 0.79 59
rs2004640 0.662 0.520 7 128938247 splice donor variant T/G snv 0.52 26
rs2104286 0.662 0.440 10 6057082 intron variant T/C snv 0.18 25
rs1980422 0.776 0.320 2 203745673 intergenic variant C/A;T snv 9