Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs1009298200 | 0.742 | 0.400 | 16 | 5079077 | missense variant | C/G;T | snv | 7.0E-06 | 34 | ||
rs1010184002 | 0.689 | 0.400 | 6 | 42978878 | stop gained | C/T | snv | 7.0E-06 | 60 | ||
rs104894229 | 0.564 | 0.600 | 11 | 534289 | missense variant | C/A;G;T | snv | 73 | |||
rs10510181 | 0.882 | 0.200 | 3 | 149364 | intron variant | G/A | snv | 0.31 | 4 | ||
rs1057518789 | 0.925 | 0.040 | 16 | 3728803 | stop gained | G/A | snv | 2 | |||
rs1057518812 | 0.827 | 0.240 | 15 | 48430742 | missense variant | T/A | snv | 6 | |||
rs1057518828 | 1.000 | 0.040 | 17 | 44911317 | missense variant | T/G | snv | 1 | |||
rs1057518891 | 0.851 | 0.120 | 8 | 60854479 | stop gained | C/T | snv | 6 | |||
rs1057518908 | 0.882 | 0.120 | 12 | 47984112 | missense variant | C/T | snv | 6 | |||
rs1057519320 | 0.807 | 0.160 | 15 | 48444574 | missense variant | G/A | snv | 7 | |||
rs1057519321 | 0.807 | 0.160 | 5 | 128349391 | missense variant | C/A;T | snv | 7 | |||
rs1057520063 | 0.763 | 0.200 | 7 | 41964641 | frameshift variant | -/A | delins | 13 | |||
rs1060505041 | 0.716 | 0.400 | 19 | 13136099 | missense variant | C/A;T | snv | 34 | |||
rs1064793575 | 0.925 | 0.040 | X | 136016706 | frameshift variant | GT/- | delins | 6 | |||
rs1085307132 | 0.882 | 0.160 | 8 | 143817668 | frameshift variant | -/TTTT | delins | 5 | |||
rs1085308004 | 0.807 | 0.240 | 15 | 48425420 | missense variant | A/G | snv | 9 | |||
rs1085308052 | 0.851 | 0.160 | 10 | 87952144 | frameshift variant | -/T | delins | 5 | |||
rs1114167445 | 0.851 | 0.160 | 19 | 40504064 | stop gained | C/T | snv | 8.0E-06 | 15 | ||
rs11190870 | 0.827 | 0.200 | 10 | 101219450 | intergenic variant | T/A;C | snv | 6 | |||
rs112550005 | 0.742 | 0.240 | 15 | 48425829 | stop gained | G/A | snv | 18 | |||
rs113422242 | 0.763 | 0.240 | 15 | 48510065 | stop gained | G/A | snv | 7.0E-06 | 14 | ||
rs113871094 | 0.683 | 0.320 | 15 | 48465820 | stop gained | G/A | snv | 34 | |||
rs11598177 | 1.000 | 0.040 | 10 | 101220399 | regulatory region variant | T/C | snv | 0.47 | 1 | ||
rs1163944538 | 0.641 | 0.560 | 17 | 75494905 | frameshift variant | -/A | delins | 4.0E-06 | 73 | ||
rs1178187217 | 0.683 | 0.480 | 7 | 21600085 | missense variant | G/A;T | snv | 4.3E-06 | 38 |