| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs115169993 | 1.000 | 0.040 | 1 | 162772032 | missense variant | G/A | snv | 7.8E-04 | 2.9E-03 | 1 | |
| rs116150891 | 1.000 | 0.040 | 9 | 21970929 | missense variant | G/A;C | snv | 5.6E-04 | 2.6E-03 | 1 | |
| rs11707807 | 1.000 | 0.040 | 3 | 188370473 | intron variant | A/G | snv | 0.36 | 1 | ||
| rs117984432 | 1.000 | 0.040 | 16 | 89388583 | intron variant | T/C | snv | 2.0E-02 | 1 | ||
| rs121913230 | 1.000 | 0.040 | 7 | 55181437 | missense variant | G/A | snv | 1 | |||
| rs121913431 | 1.000 | 0.040 | 7 | 55181438 | missense variant | G/A | snv | 1 | |||
| rs1295445617 | 1.000 | 0.040 | 2 | 47403398 | synonymous variant | G/A;C;T | snv | 4.5E-06; 4.5E-06 | 1 | ||
| rs1327891278 | 1.000 | 0.040 | 8 | 55950487 | missense variant | C/G | snv | 4.0E-06 | 7.0E-06 | 1 | |
| rs13301660 | 1.000 | 0.040 | 9 | 136446350 | intron variant | C/T | snv | 0.20 | 1 | ||
| rs1460816 | 1.000 | 0.040 | 13 | 32354271 | intron variant | G/A | snv | 0.54 | 1 | ||
| rs149906873 | 1.000 | 0.040 | 15 | 28088564 | intron variant | G/A | snv | 1 | |||
| rs1607237 | 1.000 | 0.040 | 3 | 179232509 | intron variant | C/T | snv | 0.68 | 1 | ||
| rs201125580 | 1.000 | 0.040 | 9 | 95467191 | missense variant | C/A;T | snv | 4.0E-06; 3.8E-04 | 1 | ||
| rs2233914 | 1.000 | 0.040 | 9 | 113221260 | 5 prime UTR variant | G/A | snv | 0.16 | 0.13 | 1 | |
| rs2298211 | 1.000 | 0.040 | 1 | 1211863 | intron variant | A/C | snv | 8.1E-02 | 8.2E-02 | 1 | |
| rs35324266 | 1.000 | 0.040 | 6 | 32625467 | upstream gene variant | C/T | snv | 0.16 | 1 | ||
| rs3732183 | 1.000 | 0.040 | 2 | 47466820 | intron variant | G/A;T | snv | 0.34; 4.0E-06 | 0.40 | 1 | |
| rs4455710 | 1.000 | 0.040 | 6 | 32641081 | intron variant | C/T | snv | 0.22 | 1 | ||
| rs454421 | 1.000 | 0.040 | 19 | 45341392 | intron variant | C/G;T | snv | 0.44 | 1 | ||
| rs45549733 | 1.000 | 0.040 | 11 | 67586503 | missense variant | C/G;T | snv | 7.6E-05 | 1 | ||
| rs470558 | 1.000 | 0.040 | 11 | 102795585 | synonymous variant | T/C | snv | 0.92 | 0.95 | 1 | |
| rs532172691 | 1.000 | 0.040 | 1 | 153563811 | stop gained | G/A | snv | 2.2E-04 | 3.4E-04 | 1 | |
| rs5854 | 1.000 | 0.040 | 11 | 102790143 | 3 prime UTR variant | G/A | snv | 0.29 | 1 | ||
| rs62209647 | 1.000 | 0.040 | 20 | 33917852 | upstream gene variant | G/C | snv | 4.4E-02 | 1 | ||
| rs62246017 | 1.000 | 0.040 | 3 | 71433933 | intron variant | G/A;C | snv | 1 |