| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs4588 | 0.597 | 0.720 | 4 | 71752606 | missense variant | G/A;T | snv | 1.6E-05; 0.25 | 2 | ||
| rs526126 | 1.000 | 0.040 | 11 | 61857413 | intron variant | G/C;T | snv | 0.81; 8.0E-06 | 2 | ||
| rs7341475 | 0.851 | 0.240 | 7 | 103764368 | intron variant | G/A | snv | 0.17 | 2 | ||
| rs870142 | 0.851 | 0.120 | 4 | 4646320 | intron variant | C/G;T | snv | 2 | |||
| rs886037776 | 0.925 | 0.280 | 9 | 137817477 | stop gained | G/A | snv | 2 | |||
| rs10497655 | 1.000 | 0.040 | 2 | 184597314 | intron variant | T/C;G | snv | 1 | |||
| rs10498676 | 0.925 | 0.040 | 6 | 11026766 | intron variant | G/A | snv | 0.18 | 1 | ||
| rs1131692040 | 0.882 | 0.160 | X | 154399844 | missense variant | A/G | snv | 1 | |||
| rs121908445 | 0.925 | 0.040 | 7 | 148147542 | missense variant | T/C | snv | 3.3E-04 | 1.7E-04 | 1 | |
| rs1276388879 | 1.000 | 0.040 | 1 | 151405647 | missense variant | A/C;G | snv | 1 | |||
| rs1372713010 | 1.000 | 0.040 | 1 | 151428041 | missense variant | G/A | snv | 1 | |||
| rs1396313317 | 1.000 | 0.040 | 7 | 147562137 | splice acceptor variant | G/A;C | snv | 4.0E-06 | 1 | ||
| rs1418634444 | 1.000 | 0.040 | 1 | 151408777 | missense variant | T/C | snv | 7.0E-06 | 1 | ||
| rs1452048149 | 1.000 | 0.040 | 1 | 151404828 | missense variant | C/T | snv | 4.0E-06 | 1 | ||
| rs1476293577 | 1.000 | 0.040 | 1 | 151428188 | missense variant | G/A;C | snv | 1 | |||
| rs1484207450 | 1.000 | 0.040 | 1 | 151405155 | missense variant | A/G | snv | 7.0E-06 | 1 | ||
| rs1557863430 | 1.000 | 0.040 | 1 | 151405229 | missense variant | T/C | snv | 1 | |||
| rs1557863440 | 1.000 | 0.040 | 1 | 151405233 | missense variant | T/C | snv | 1 | |||
| rs1557863546 | 1.000 | 0.040 | 1 | 151405263 | missense variant | T/A | snv | 1 | |||
| rs1557867853 | 1.000 | 0.040 | 1 | 151406330 | missense variant | G/A | snv | 1 | |||
| rs1557870645 | 1.000 | 0.040 | 1 | 151407271 | missense variant | C/T | snv | 1 | |||
| rs1557874046 | 1.000 | 0.040 | 1 | 151408807 | missense variant | T/G | snv | 1 | |||
| rs1557901347 | 1.000 | 0.040 | 1 | 151424027 | missense variant | G/C | snv | 1 | |||
| rs1557902023 | 1.000 | 0.040 | 1 | 151424154 | missense variant | G/C | snv | 1 | |||
| rs1557909572 | 1.000 | 0.040 | 1 | 151427931 | missense variant | G/C | snv | 1 |