| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs11977670 | 1.000 | 0.080 | 7 | 140242504 | downstream gene variant | G/A | snv | 0.39 | 1 | ||
| rs1236971182 | 1.000 | 0.080 | 6 | 36684381 | missense variant | C/T | snv | 8.1E-06 | 1 | ||
| rs2143416 | 1.000 | 0.080 | 1 | 186684633 | upstream gene variant | A/C;T | snv | 0.27 | 1 | ||
| rs62355902 | 1.000 | 0.080 | 5 | 56757896 | intergenic variant | A/T | snv | 0.15 | 1 | ||
| rs6453204 | 1.000 | 0.080 | 5 | 76143375 | intron variant | A/G | snv | 0.90 | 1 | ||
| rs6569648 | 1.000 | 0.080 | 6 | 130027974 | intron variant | C/T | snv | 0.84 | 1 | ||
| rs747097215 | 1.000 | 0.080 | 7 | 100856990 | missense variant | C/T | snv | 2.0E-05 | 2.1E-05 | 1 | |
| rs757172284 | 1.000 | 0.080 | 16 | 56340838 | missense variant | G/A | snv | 1.6E-05 | 1 | ||
| rs762292600 | 0.925 | 0.080 | 6 | 151944316 | missense variant | A/G | snv | 4.0E-06 | 1.4E-05 | 7 | |
| rs200863613 | 0.925 | 0.080 | 9 | 21971061 | missense variant | C/A;T | snv | 8.5E-05 | 3.7E-04 | 6 | |
| rs752295912 | 0.925 | 0.080 | 17 | 39710398 | missense variant | C/T | snv | 1.6E-05 | 6 | ||
| rs11544331 | 0.925 | 0.080 | 7 | 1091775 | missense variant | C/T | snv | 0.21 | 0.19 | 5 | |
| rs180177111 | 0.925 | 0.080 | 16 | 23629831 | stop gained | G/A | snv | 4.0E-06 | 5 | ||
| rs570613 | 0.925 | 0.080 | 10 | 8064539 | intron variant | C/T | snv | 0.60 | 5 | ||
| rs10109984 | 0.925 | 0.080 | 8 | 47891114 | intron variant | T/C | snv | 0.54 | 4 | ||
| rs1056123575 | 0.925 | 0.080 | 21 | 26844557 | missense variant | G/A | snv | 4.2E-06 | 7.0E-06 | 4 | |
| rs1114167628 | 0.925 | 0.080 | 10 | 87961033 | stop gained | -/ATATCTAG | delins | 4 | |||
| rs11552449 | 0.925 | 0.080 | 1 | 113905767 | missense variant | C/G;T | snv | 0.22 | 0.15 | 4 | |
| rs1172398253 | 0.925 | 0.080 | 1 | 85582045 | missense variant | C/T | snv | 4.0E-06 | 4 | ||
| rs11780156 | 0.925 | 0.080 | 8 | 128182395 | intron variant | C/T | snv | 0.13 | 4 | ||
| rs11895168 | 0.925 | 0.080 | 2 | 211377467 | 3 prime UTR variant | A/C | snv | 0.68 | 4 | ||
| rs12945597 | 0.925 | 0.080 | 17 | 18271367 | downstream gene variant | G/A | snv | 0.31 | 4 | ||
| rs13283662 | 0.925 | 0.080 | 9 | 6428530 | intron variant | T/C | snv | 4 | |||
| rs1364963022 | 0.925 | 0.080 | 6 | 151944233 | missense variant | G/C | snv | 4.0E-06 | 4 | ||
| rs141613848 | 0.925 | 0.080 | 17 | 74768481 | missense variant | A/T | snv | 1.0E-03 | 1.2E-03 | 4 |