Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1217691063 0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 614
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
rs34637584 0.583 0.480 12 40340400 missense variant G/A snv 5.3E-04 3.6E-04 78
rs104893877 0.614 0.360 4 89828149 missense variant C/T snv 59
rs74315401 0.683 0.320 20 4699525 missense variant C/T snv 32
rs75932628 0.662 0.480 6 41161514 missense variant C/A;T snv 6.8E-05; 2.6E-03 28
rs63750756 0.716 0.200 17 46010324 missense variant T/G snv 2.6E-05 23
rs5848 0.708 0.120 17 44352876 3 prime UTR variant C/T snv 0.41 17
rs63751438 0.776 0.120 17 46010388 missense variant C/T snv 16
rs17125721 0.763 0.120 14 73206470 missense variant A/G snv 1.5E-02 1.5E-02 14
rs104893875 0.742 0.120 4 89828170 missense variant C/T snv 4.0E-06 13
rs63750376 0.827 0.120 17 45996657 missense variant G/T snv 7
rs63751068 0.827 0.120 14 73186920 missense variant G/C;T snv 6