Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs121909224 0.627 0.560 10 87933147 stop gained C/G;T snv 1.2E-05 35
rs121909231 0.667 0.600 10 87961095 stop gained C/A;T snv 29
rs121909219 0.689 0.400 10 87957915 stop gained C/A;T snv 24
rs121909229 0.683 0.400 10 87933148 missense variant G/A;C;T snv 23
rs121913294 0.776 0.280 10 87952143 missense variant G/A;C;T snv 8.0E-06 11
rs398123318 0.776 0.240 10 87925558 splice region variant AGTA/- delins 9
rs398123316 0.851 0.160 10 87925530 missense variant A/G;T snv 8
rs786201044 0.827 0.200 10 87933165 missense variant T/C snv 6
rs1057517809 0.882 0.160 10 87965286 splice acceptor variant G/A;C snv 4
rs1057519368 0.882 0.320 10 87957958 stop gained T/A;C;G snv 4.0E-06 4
rs146650273 0.882 0.160 10 87961042 frameshift variant ACTT/- delins 4
rs587782360 0.851 0.280 10 87933162 missense variant A/G snv 4
rs786201995 1.000 0.120 10 87864539 missense variant G/A;C;T snv 2
rs876660507 1.000 0.120 10 87952134 missense variant G/T snv 2
rs1564566861 1.000 0.120 10 87957933 frameshift variant A/- del 1
rs1564570283 1.000 0.120 10 87965294 frameshift variant TGTACTTCACAAAAACA/- del 1
rs1564814454 1.000 0.120 10 87894047 frameshift variant T/- del 1
rs1564826829 1.000 0.120 10 87925556 frameshift variant -/T delins 1
rs1564830444 1.000 0.120 10 87933217 frameshift variant -/TT delins 1
rs1564838034 1.000 0.120 10 87952250 frameshift variant G/- delins 1
rs1564801750 1.000 0.120 10 87864512 frameshift variant -/G delins 1