Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs1445362103 | 1.000 | 0.040 | 13 | 111244248 | missense variant | T/C | snv | 1.2E-05 | 7.0E-06 | 2 | |
rs752411521 | 1.000 | 0.040 | 20 | 33624825 | missense variant | T/C | snv | 4.0E-06 | 1 | ||
rs587777260 | 0.925 | 0.080 | 13 | 75359852 | stop gained | G/A;T | snv | 4.0E-06 | 2 | ||
rs587779383 | 0.851 | 0.120 | 4 | 1806157 | missense variant | A/C;G;T | snv | 5 | |||
rs121913135 | 0.882 | 0.120 | 19 | 7125437 | missense variant | C/A | snv | 3 | |||
rs28931615 | 0.732 | 0.240 | 4 | 1804426 | missense variant | C/A;T | snv | 13 | |||
rs2963 | 0.851 | 0.240 | 19 | 7163143 | synonymous variant | G/A | snv | 9.8E-02 | 0.13 | 4 | |
rs1014959895 | 0.763 | 0.360 | 16 | 68329105 | stop gained | G/C;T | snv | 4.0E-06; 1.6E-05 | 16 | ||
rs1251713297 | 0.776 | 0.360 | 16 | 68355785 | stop gained | C/A | snv | 8.1E-06 | 15 | ||
rs78311289 | 0.689 | 0.440 | 4 | 1806162 | missense variant | A/C;G | snv | 4.0E-06 | 25 | ||
rs121913105 | 0.653 | 0.600 | 4 | 1806163 | missense variant | A/C;T | snv | 30 |