| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs200894535 | 1.000 | 0.080 | 5 | 157530816 | missense variant | C/T | snv | 1.6E-05 | 1 | ||
| rs544557652 | 1.000 | 0.080 | 4 | 174975617 | missense variant | C/T | snv | 1.0E-04 | 9.1E-05 | 1 | |
| rs772388824 | 1.000 | 0.080 | 4 | 174976138 | missense variant | G/A | snv | 1.2E-05 | 7.0E-06 | 1 | |
| rs12140 | 1.000 | 0.080 | 21 | 26837076 | 3 prime UTR variant | T/C | snv | 7.7E-02 | 1 | ||
| rs776537988 | 1.000 | 0.080 | 11 | 130473277 | missense variant | A/G | snv | 3.6E-05 | 5.6E-05 | 1 | |
| rs368783738 | 1.000 | 0.080 | 16 | 77362176 | missense variant | C/T | snv | 1.7E-04 | 1.3E-04 | 1 | |
| rs776584074 | 1.000 | 0.080 | 16 | 77356036 | missense variant | T/C;G | snv | 1.2E-05 | 1 | ||
| rs142860011 | 1.000 | 0.080 | 15 | 83913151 | missense variant | G/A | snv | 1.6E-05 | 1.4E-05 | 1 | |
| rs1439091253 | 1.000 | 0.080 | 15 | 83885128 | missense variant | G/A | snv | 4.0E-06 | 7.0E-06 | 1 | |
| rs146769560 | 1.000 | 0.080 | 15 | 83970556 | missense variant | C/T | snv | 2.8E-05 | 2.1E-05 | 1 | |
| rs138734198 | 1.000 | 0.080 | 10 | 1217099 | missense variant | C/T | snv | 1.8E-04 | 7.0E-04 | 1 | |
| rs899207013 | 1.000 | 0.080 | 1 | 203165427 | missense variant | G/A | snv | 1.4E-05 | 1 | ||
| rs552053449 | 1.000 | 0.080 | 6 | 151349109 | missense variant | G/A | snv | 2.8E-05 | 7.0E-06 | 1 | |
| rs143517596 | 1.000 | 0.080 | 12 | 4615810 | missense variant | G/A | snv | 4.7E-04 | 4.7E-04 | 1 | |
| rs745389246 | 1.000 | 0.080 | 14 | 32823328 | missense variant | C/A | snv | 4.0E-06 | 1 | ||
| rs768309358 | 1.000 | 0.080 | 3 | 126131475 | missense variant | G/A | snv | 8.0E-06 | 7.0E-06 | 1 | |
| rs2920421 | 1.000 | 0.080 | 17 | 7003751 | intron variant | A/G | snv | 0.68 | 1 | ||
| rs1220386463 | 1.000 | 0.080 | 16 | 2528469 | missense variant | G/A | snv | 4.0E-06 | 1 | ||
| rs151041998 | 1.000 | 0.080 | 4 | 70524899 | missense variant | G/A | snv | 8.9E-03 | 7.2E-03 | 1 | |
| rs1954727 | 1.000 | 0.080 | 8 | 107250906 | 3 prime UTR variant | C/G | snv | 0.64 | 1 | ||
| rs1264054061 | 1.000 | 0.080 | 4 | 80055997 | missense variant | C/T | snv | 7.0E-06 | 1 | ||
| rs1259132664 | 1.000 | 0.080 | 15 | 29054561 | missense variant | T/C | snv | 7.0E-06 | 1 | ||
| rs1488176769 | 1.000 | 0.080 | 5 | 112707865 | missense variant | T/C | snv | 1.4E-05 | 1 | ||
| rs41116 | 1.000 | 0.080 | 5 | 112845224 | 3 prime UTR variant | T/C | snv | 0.39 | 1 | ||
| rs779998847 | 1.000 | 0.080 | 5 | 112838262 | missense variant | G/A | snv | 8.0E-06 | 1 |