Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs1060499553 | 0.827 | 0.040 | 5 | 161890983 | missense variant | G/A | snv | 6 | |||
rs1135401733 | 1.000 | 0.040 | 1 | 244856757 | stop gained | G/A | snv | 3 | |||
rs118192211 | 0.790 | 0.080 | 20 | 63439644 | missense variant | G/A;C | snv | 9 | |||
rs121909674 | 0.790 | 0.080 | 5 | 162153132 | stop gained | C/T | snv | 8 | |||
rs1392120633 | 1.000 | 0.040 | 12 | 51807223 | missense variant | C/T | snv | 4.0E-06 | 2 | ||
rs1554208945 | 0.752 | 0.240 | 6 | 87260207 | missense variant | A/C | snv | 26 | |||
rs1555889127 | 1.000 | 0.040 | 20 | 49374625 | missense variant | C/T | snv | 6 | |||
rs1555889162 | 0.882 | 0.040 | 20 | 49374931 | missense variant | G/A;C | snv | 6 | |||
rs202151337 | 0.925 | 0.160 | 12 | 51806788 | missense variant | A/G | snv | 4 | |||
rs387906686 | 0.742 | 0.320 | 2 | 165310413 | missense variant | C/A;T | snv | 23 | |||
rs397514737 | 0.882 | 0.080 | 5 | 162149153 | missense variant | G/A | snv | 4 | |||
rs587777057 | 0.827 | 0.040 | 16 | 56336744 | missense variant | G/A | snv | 8 | |||
rs587777308 | 0.763 | 0.040 | 5 | 161873196 | missense variant | G/A | snv | 14 | |||
rs796053228 | 0.882 | 0.160 | 12 | 51807100 | missense variant | C/G;T | snv | 4 | |||
rs869312702 | 0.827 | 0.160 | 9 | 128203609 | missense variant | G/A | snv | 10 | |||
rs886041715 | 0.827 | 0.040 | 16 | 56192353 | missense variant | G/A;C;T | snv | 7 | |||
rs886041874 | 1.000 | 0.040 | 1 | 119721323 | splice donor variant | T/C | snv | 4.0E-06 | 2 | ||
rs764618040 | 1.000 | 0.040 | 1 | 119726868 | missense variant | C/T | snv | 1.6E-05 | 2.1E-05 | 2 |