Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1883832 0.581 0.680 20 46118343 5 prime UTR variant T/C snv 0.75 0.80 52
rs4810485 0.732 0.480 20 46119308 intron variant T/A;G snv 16
rs1535045 0.742 0.360 20 46119460 intron variant C/A;G;T snv 12
rs772829518 0.925 0.200 20 46122699 missense variant T/C snv 4.0E-06 2
rs4239702 1.000 0.120 20 46120612 intron variant T/C snv 0.75 1