Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs5443 | 0.532 | 0.760 | 12 | 6845711 | synonymous variant | C/T | snv | 0.36 | 0.44 | 106 | |
rs1042714 | 0.597 | 0.640 | 5 | 148826910 | stop gained | G/C;T | snv | 0.68 | 54 | ||
rs1801253 | 0.683 | 0.440 | 10 | 114045297 | missense variant | G/C | snv | 0.74 | 0.69 | 34 | |
rs1805127 | 0.732 | 0.240 | 21 | 34449523 | missense variant | T/C | snv | 0.64 | 2.0E-04 | 17 | |
rs45546039 | 0.732 | 0.120 | 3 | 38613781 | missense variant | C/A;T | snv | 4.1E-06 | 15 | ||
rs766265889 | 0.827 | 0.240 | 2 | 178535508 | stop gained | G/A;T | snv | 8.0E-06; 4.0E-06 | 11 | ||
rs3745297 | 0.790 | 0.120 | 19 | 49154952 | missense variant | A/C | snv | 0.41 | 0.38 | 10 | |
rs120074192 | 0.763 | 0.120 | 11 | 2527959 | missense variant | A/G | snv | 10 | |||
rs7626962 | 0.790 | 0.080 | 3 | 38579416 | missense variant | G/A;T | snv | 1.6E-05; 5.9E-03 | 10 | ||
rs3766871 | 0.790 | 0.240 | 1 | 237614784 | missense variant | G/A;T | snv | 4.0E-02 | 9 | ||
rs104894503 | 0.776 | 0.160 | 15 | 63060899 | missense variant | G/A | snv | 1.6E-05 | 2.8E-05 | 9 | |
rs794728708 | 0.827 | 0.120 | 1 | 237377386 | missense variant | G/A;T | snv | 8 | |||
rs104894580 | 0.790 | 0.240 | 17 | 70175238 | missense variant | C/A;T | snv | 4.0E-06 | 7 | ||
rs199473605 | 0.851 | 0.120 | 3 | 38560374 | missense variant | C/G;T | snv | 4.8E-05; 4.0E-06 | 7 | ||
rs56984562 | 0.827 | 0.200 | 1 | 156137666 | missense variant | C/A;G;T | snv | 6 | |||
rs137854600 | 0.807 | 0.120 | 3 | 38551504 | missense variant | C/A;T | snv | 6 | |||
rs1860561 | 0.851 | 0.080 | 12 | 110345436 | intron variant | G/A | snv | 0.19 | 5 | ||
rs104894584 | 0.851 | 0.120 | 17 | 70175553 | missense variant | G/A | snv | 5 | |||
rs121918600 | 0.882 | 0.080 | 1 | 237791441 | missense variant | C/T | snv | 5 | |||
rs59301204 | 0.925 | 0.080 | 1 | 156135956 | missense variant | G/A;C | snv | 1.2E-05 | 4 | ||
rs755373114 | 0.925 | 0.080 | 4 | 113341742 | missense variant | A/C | snv | 7.2E-05 | 3 | ||
rs192749597 | 0.882 | 0.080 | 12 | 2679712 | missense variant | C/T | snv | 9.2E-04 | 3.5E-03 | 3 | |
rs1805120 | 0.882 | 0.080 | 7 | 150952443 | synonymous variant | G/A | snv | 0.30 | 0.26 | 3 | |
rs120074187 | 0.882 | 0.120 | 11 | 2572963 | missense variant | G/A | snv | 4.8E-05 | 2.1E-05 | 3 | |
rs761056344 | 0.925 | 0.080 | 6 | 118558994 | missense variant | C/G;T | snv | 4.0E-06; 3.2E-05 | 3 |