Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs6265 0.436 0.760 11 27658369 missense variant C/T snv 0.19 0.15 272
rs759834365 0.448 0.760 11 27658456 missense variant C/T snv 1.2E-05 237
rs1800795 0.494 0.840 7 22727026 intron variant C/G snv 0.71 140
rs104893877 0.614 0.360 4 89828149 missense variant C/T snv 59
rs63751273 0.645 0.280 17 46010389 missense variant C/T snv 42
rs6295 0.645 0.200 5 63962738 intron variant C/G snv 0.49 40
rs1018381 0.882 0.040 6 15656839 intron variant G/A snv 0.16 6