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
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
rs16969968 0.653 0.360 15 78590583 missense variant G/A snv 0.26 0.24 37
rs63750424 0.677 0.240 17 46024061 missense variant C/T snv 1.6E-05 30
rs5522 0.732 0.320 4 148436323 missense variant C/T snv 0.88 0.89 19