| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs397508139 | 0.882 | 0.160 | 7 | 117540237 | missense variant | T/A;C | snv | 4.0E-06; 4.0E-06 | 1 | ||
| rs397508315 | 1.000 | 0.120 | 7 | 117592027 | missense variant | T/G | snv | 1 | |||
| rs121909044 | 0.925 | 0.200 | 7 | 117587812 | missense variant | G/A;C | snv | 4.0E-06 | 1 | ||
| rs150691494 | 1.000 | 0.120 | 7 | 117540132 | missense variant | A/G | snv | 2.9E-04 | 1.8E-04 | 1 | |
| rs75549581 | 0.925 | 0.160 | 7 | 117587829 | missense variant | G/A;T | snv | 2.0E-05; 4.0E-06 | 1 | ||
| rs139304906 | 0.925 | 0.160 | 7 | 117611671 | missense variant | T/C | snv | 4.0E-06 | 7.0E-06 | 1 | |
| rs77902683 | 1.000 | 0.120 | 7 | 117642568 | missense variant | G/A;T | snv | 4.0E-06 | 1 | ||
| rs193922504 | 1.000 | 0.120 | 7 | 117587827 | missense variant | T/C | snv | 4.0E-06 | 7.0E-06 | 1 | |
| rs397508314 | 1.000 | 0.120 | 7 | 117592026 | missense variant | A/C;G;T | snv | 8.6E-06; 4.3E-06 | 1 | ||
| rs397508621 | 1.000 | 0.120 | 7 | 117642592 | missense variant | A/G | snv | 4.0E-06 | 1 | ||
| rs121909016 | 1.000 | 0.120 | 7 | 117540163 | missense variant | C/G | snv | 1 | |||
| rs397508282 | 1.000 | 0.120 | 7 | 117590387 | missense variant | G/A | snv | 1 | |||
| rs397508276 | 0.925 | 0.160 | 7 | 117590378 | missense variant | T/C;G | snv | 9.6E-05 | 1 | ||
| rs397508480 | 0.925 | 0.160 | 7 | 117610547 | missense variant | C/A | snv | 4.0E-06 | 1 | ||
| rs121908803 | 0.925 | 0.160 | 7 | 117535281 | missense variant | C/A;T | snv | 4.0E-06 | 7.0E-06 | 1 | |
| rs397508146 | 1.000 | 0.120 | 7 | 117540267 | missense variant | T/C | snv | 1 | |||
| rs397508280 | 1.000 | 0.120 | 7 | 117590385 | missense variant | T/C | snv | 1 | |||
| rs201978662 | 1.000 | 0.120 | 7 | 117592004 | missense variant | G/A | snv | 7.0E-06 | 1 | ||
| rs397508819 | 1.000 | 0.120 | 7 | 117540170 | missense variant | G/C;T | snv | 1 | |||
| rs34911792 | 0.925 | 0.160 | 7 | 117627758 | missense variant | T/G | snv | 5.0E-03 | 5.7E-03 | 1 | |
| rs121909020 | 1.000 | 0.120 | 7 | 117611640 | missense variant | G/A;C | snv | 4.0E-06 | 1 | ||
| rs397508635 | 0.925 | 0.160 | 7 | 117480132 | missense variant | C/A;T | snv | 1 | |||
| rs397508316 | 1.000 | 0.120 | 7 | 117592049 | missense variant | G/A;C | snv | 4.1E-06 | 1 | ||
| rs121909005 | 0.851 | 0.160 | 7 | 117587801 | missense variant | T/A;C;G | snv | 4.0E-06; 8.0E-06 | 1 | ||
| rs200553511 | 1.000 | 0.120 | 7 | 117610614 | missense variant | G/A;T | snv | 4.0E-06 | 1 |