| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs121909017 | 0.851 | 0.160 | 7 | 117559546 | missense variant | C/T | snv | 8.0E-06 | 4 | ||
| rs35516286 | 0.851 | 0.160 | 7 | 117531068 | missense variant | T/A;C | snv | 1.8E-03 | 4 | ||
| rs397508464 | 0.851 | 0.160 | 7 | 117530918 | missense variant | A/C;G | snv | 8.0E-06 | 4 | ||
| rs397508759 | 0.851 | 0.160 | 7 | 117534363 | stop gained | G/A;T | snv | 4.0E-06 | 4 | ||
| rs397508778 | 0.851 | 0.160 | 7 | 117535326 | stop gained | C/T | snv | 4.0E-06 | 4 | ||
| rs75039782 | 0.851 | 0.160 | 7 | 117639961 | intron variant | C/G;T | snv | 4 | |||
| rs77284892 | 0.851 | 0.160 | 7 | 117509047 | stop gained | G/A;T | snv | 2.4E-05 | 4 | ||
| rs77646904 | 0.851 | 0.160 | 7 | 117559629 | missense variant | G/A;T | snv | 1.5E-04; 4.0E-06 | 4 | ||
| rs77834169 | 0.851 | 0.160 | 7 | 117530974 | missense variant | C/A;G;T | snv | 8.0E-06; 2.0E-05; 2.0E-04 | 4 | ||
| rs78802634 | 0.851 | 0.160 | 7 | 117611707 | stop gained | G/A | snv | 2.4E-05 | 4 | ||
| rs79282516 | 0.851 | 0.160 | 7 | 117559509 | missense variant | G/A;T | snv | 4 | |||
| rs80055610 | 0.851 | 0.160 | 7 | 117587833 | missense variant | G/A;C | snv | 2.4E-05 | 4 | ||
| rs80282562 | 0.851 | 0.160 | 7 | 117534318 | missense variant | G/A | snv | 1.6E-05 | 4 | ||
| rs113993958 | 0.882 | 0.200 | 7 | 117530953 | missense variant | G/A;C;T | snv | 2.0E-05; 4.0E-06 | 3 | ||
| rs11971167 | 0.882 | 0.160 | 7 | 117642528 | missense variant | G/A;T | snv | 1.3E-03 | 3 | ||
| rs121908755 | 0.882 | 0.200 | 7 | 117587800 | missense variant | G/A;T | snv | 8.8E-05 | 3 | ||
| rs121908757 | 0.925 | 0.160 | 7 | 117587799 | missense variant | A/C | snv | 4.0E-06 | 3 | ||
| rs1805177 | 0.925 | 0.160 | 7 | 117548629 | splice acceptor variant | TTTTTT/-;TTTT;TTTTT;TTTTTTT;TTTTTTTT;TTTTTTTTT;TTTTTTTTTTT;TTTTTTTTTTTTT | delins | 3 | |||
| rs201124247 | 0.882 | 0.160 | 7 | 117592008 | missense variant | A/G | snv | 3.1E-05 | 3 | ||
| rs397508139 | 0.882 | 0.160 | 7 | 117540237 | missense variant | T/A;C | snv | 4.0E-06; 4.0E-06 | 3 | ||
| rs397508288 | 0.882 | 0.200 | 7 | 117590409 | missense variant | A/C;G | snv | 4.0E-06 | 3 | ||
| rs58598099 | 0.882 | 0.200 | 16 | 2116917 | missense variant | A/G | snv | 3 | |||
| rs74571530 | 0.882 | 0.160 | 7 | 117559594 | missense variant | T/A;C;G | snv | 9.4E-04 | 3 | ||
| rs75389940 | 0.882 | 0.120 | 7 | 117627753 | missense variant | A/G | snv | 4.0E-06 | 3 | ||
| rs1057516457 | 0.925 | 0.160 | 7 | 117664711 | frameshift variant | CA/- | delins | 2 |