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
rs671 0.529 0.840 12 111803962 missense variant G/A snv 1.9E-02 5.8E-03 116
rs4633 0.695 0.400 22 19962712 synonymous variant C/T snv 0.46 0.45 25
rs10767664 0.752 0.400 11 27704439 intron variant T/A snv 0.83 16
rs11030104 0.790 0.240 11 27662970 intron variant A/G snv 0.16 12