| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs748676559 | 0.925 | 0.080 | 17 | 37284932 | missense variant | C/T | snv | 4.0E-06 | 2.1E-05 | 3 | |
| rs1277892620 | 0.925 | 0.120 | 17 | 37242036 | synonymous variant | A/G | snv | 4.0E-06 | 7.0E-06 | 2 | |
| rs1395589486 | 0.925 | 0.080 | 17 | 37258316 | missense variant | A/G | snv | 4.0E-06 | 2 | ||
| rs11651239 | 1.000 | 0.040 | 17 | 37139167 | intron variant | G/A | snv | 0.20 | 1 | ||
| rs1172063879 | 1.000 | 0.040 | 17 | 37259427 | missense variant | C/T | snv | 4.0E-06 | 1 | ||
| rs1233948559 | 1.000 | 0.080 | 17 | 37161868 | synonymous variant | T/C | snv | 8.0E-06 | 1 | ||
| rs12449696 | 1.000 | 0.040 | 17 | 37095363 | intron variant | C/T | snv | 0.22 | 1 | ||
| rs12450937 | 1.000 | 0.040 | 17 | 37137586 | intron variant | C/T | snv | 0.51 | 1 | ||
| rs12453407 | 17 | 37232521 | intron variant | A/G | snv | 0.65 | 1 | ||||
| rs1266175 | 17 | 37111115 | intron variant | A/G | snv | 0.54 | 1 | ||||
| rs1357271377 | 1.000 | 0.080 | 17 | 37161959 | missense variant | C/T | snv | 1.6E-05 | 1 | ||
| rs17573357 | 1.000 | 0.040 | 17 | 37119704 | intron variant | A/G | snv | 8.5E-02 | 1 | ||
| rs1900101 | 1.000 | 0.040 | 17 | 37098342 | intron variant | T/G | snv | 0.30 | 1 | ||
| rs2106772 | 1.000 | 0.040 | 17 | 37104485 | intron variant | C/T | snv | 0.24 | 1 | ||
| rs2229416 | 17 | 37252940 | synonymous variant | C/T | snv | 0.18 | 0.12 | 1 | |||
| rs2542670 | 1.000 | 0.040 | 17 | 37294135 | intron variant | A/G;T | snv | 1 | |||
| rs7208415 | 1.000 | 0.040 | 17 | 37132758 | intron variant | G/A | snv | 0.17 | 1 | ||
| rs7215365 | 1.000 | 0.040 | 17 | 37118979 | intron variant | C/A;T | snv | 1 | |||
| rs73982299 | 1.000 | 0.080 | 17 | 37274293 | missense variant | C/T | snv | 2.3E-04 | 9.3E-04 | 1 | |
| rs755418013 | 1.000 | 0.040 | 17 | 37130209 | missense variant | G/A | snv | 4.0E-06 | 1 | ||
| rs758980216 | 1.000 | 0.040 | 17 | 37149965 | missense variant | G/A | snv | 1.2E-05 | 2.8E-05 | 1 | |
| rs775831954 | 1.000 | 0.080 | 17 | 37248015 | missense variant | C/T | snv | 4.0E-06 | 7.0E-06 | 1 | |
| rs9897583 | 1.000 | 0.040 | 17 | 37113716 | intron variant | C/G | snv | 0.34 | 1 | ||
| rs9906044 | 17 | 37251740 | intron variant | A/T | snv | 0.49 | 1 | ||||
| rs9906543 | 17 | 37162308 | intron variant | T/A;C | snv | 1 |