| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs113993959 | 0.677 | 0.280 | 7 | 117587778 | stop gained | G/A;T | snv | 8.0E-06; 3.4E-04 | 19 | ||
| rs74597325 | 0.708 | 0.320 | 7 | 117587811 | stop gained | C/G;T | snv | 6.8E-05 | 16 | ||
| rs113993960 | 0.827 | 0.160 | 7 | 117559591 | inframe deletion | CTT/- | delins | 8.0E-03 | 6 | ||
| rs121908761 | 0.851 | 0.160 | 7 | 117611717 | stop gained | C/A;G | snv | 1.2E-05 | 4 | ||
| rs121909005 | 0.851 | 0.160 | 7 | 117587801 | missense variant | T/A;C;G | snv | 4.0E-06; 8.0E-06 | 4 | ||
| rs121908753 | 0.851 | 0.160 | 7 | 117540285 | missense variant | G/A | snv | 2.4E-05 | 4 | ||
| rs77010898 | 0.742 | 0.280 | 7 | 117642566 | stop gained | G/A;C | snv | 4.6E-04; 4.0E-06 | 4 | ||
| rs267606723 | 0.827 | 0.200 | 7 | 117642451 | missense variant | G/A;T | snv | 8.0E-06; 4.0E-06 | 4 | ||
| rs75096551 | 0.851 | 0.160 | 7 | 117606754 | splice donor variant | G/A;C;T | snv | 1.0E-04 | 2.9E-04 | 4 | |
| rs78756941 | 0.851 | 0.160 | 7 | 117531115 | splice donor variant | G/T | snv | 7.7E-05 | 1.0E-04 | 4 | |
| rs397508464 | 0.851 | 0.160 | 7 | 117530918 | missense variant | A/C;G | snv | 8.0E-06 | 4 | ||
| rs121908802 | 0.851 | 0.160 | 7 | 117535263 | missense variant | C/T | snv | 7.0E-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 | ||
| rs121908759 | 0.827 | 0.160 | 7 | 117592032 | missense variant | G/A | snv | 1.0E-04 | 3.8E-04 | 4 | |
| rs79850223 | 0.851 | 0.160 | 7 | 117627525 | stop gained | C/T | snv | 3.2E-05 | 2.8E-05 | 4 | |
| rs397508759 | 0.851 | 0.160 | 7 | 117534363 | stop gained | G/A;T | snv | 4.0E-06 | 4 | ||
| rs75039782 | 0.851 | 0.160 | 7 | 117639961 | intron variant | C/G;T | snv | 4 | |||
| rs121909011 | 0.807 | 0.160 | 7 | 117540230 | missense variant | C/T | snv | 5.6E-05 | 9.1E-05 | 4 | |
| rs77284892 | 0.851 | 0.160 | 7 | 117509047 | stop gained | G/A;T | snv | 2.4E-05 | 4 | ||
| rs78655421 | 0.716 | 0.240 | 7 | 117530975 | missense variant | G/A;C;T | snv | 1.5E-03; 1.2E-05 | 4 | ||
| rs78802634 | 0.851 | 0.160 | 7 | 117611707 | stop gained | G/A | snv | 2.4E-05 | 4 | ||
| rs397508778 | 0.851 | 0.160 | 7 | 117535326 | stop gained | C/T | snv | 4.0E-06 | 4 | ||
| rs80282562 | 0.851 | 0.160 | 7 | 117534318 | missense variant | G/A | snv | 1.6E-05 | 4 | ||
| rs75527207 | 0.732 | 0.440 | 7 | 117587806 | missense variant | G/A | snv | 1.8E-04 | 3.0E-04 | 4 | |
| rs80224560 | 0.851 | 0.160 | 7 | 117602868 | splice region variant | G/A | snv | 7.6E-05 | 6.3E-05 | 4 |