| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs1217691063 | 0.330 | 0.920 | 1 | 11796309 | missense variant | A/G | snv | 4.0E-06 | 7.0E-06 | 614 | |
| rs397507444 | 0.405 | 0.880 | 1 | 11794407 | missense variant | T/G | snv | 306 | |||
| rs1801133 | 0.472 | 0.880 | 1 | 11796321 | missense variant | G/A | snv | 0.31 | 0.27 | 174 | |
| rs1805087 | 0.496 | 0.800 | 1 | 236885200 | missense variant | A/G | snv | 0.20 | 0.21 | 135 | |
| rs878853161 | 0.851 | 0.240 | 1 | 42929977 | frameshift variant | AT/- | del | 7 | |||
| rs2745557 | 0.807 | 0.200 | 1 | 186680089 | intron variant | A/G | snv | 0.83 | 6 | ||
| rs12037377 | 1.000 | 0.040 | 1 | 246551218 | missense variant | G/A | snv | 3.2E-03 | 1.6E-03 | 2 | |
| rs1477437491 | 0.925 | 0.040 | 1 | 162367213 | missense variant | G/A | snv | 2.8E-05 | 2 | ||
| rs1186689 | 1.000 | 0.040 | 1 | 160053263 | intron variant | G/T | snv | 0.49 | 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 | |||
| rs141560292 | 1.000 | 0.040 | 1 | 162154408 | missense variant | G/A | snv | 1.6E-05 | 7.7E-05 | 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 |