Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs352140 0.630 0.680 3 52222681 synonymous variant C/A;G;T snv 2.0E-05; 0.49 42
rs1015164 0.925 3 46410189 intron variant A/C;G;T snv 8
rs2227513 1.000 0.080 12 68253559 intron variant T/C snv 0.15 3