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
rs187084 0.641 0.480 3 52227015 intron variant A/G snv 0.38 36
rs5743836 0.658 0.440 3 52226766 intron variant A/G snv 0.20 31
rs352139 0.732 0.320 3 52224356 intron variant T/C snv 0.51 0.54 18