| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs115545701 | 0.925 | 0.160 | 7 | 117509089 | missense variant | C/T | snv | 1.5E-03 | 4.3E-03 | 2 | |
| rs151048781 | 0.925 | 0.160 | 7 | 117603730 | missense variant | G/A;C | snv | 5.6E-05; 8.0E-05 | 2 | ||
| rs1800097 | 0.925 | 0.160 | 7 | 117590357 | missense variant | G/A;C | snv | 1.4E-04; 4.8E-05 | 2 | ||
| rs397508759 | 0.851 | 0.160 | 7 | 117534363 | stop gained | G/A;T | snv | 4.0E-06 | 2 | ||
| rs121909011 | 0.807 | 0.160 | 7 | 117540230 | missense variant | C/T | snv | 5.6E-05 | 9.1E-05 | 2 | |
| rs75541969 | 0.827 | 0.200 | 7 | 117614699 | missense variant | G/C | snv | 4.0E-04 | 3.2E-04 | 2 | |
| rs1800111 | 0.882 | 0.160 | 7 | 117610521 | missense variant | G/C | snv | 2.3E-03 | 2.1E-03 | 2 | |
| rs113993958 | 0.882 | 0.200 | 7 | 117530953 | missense variant | G/A;C;T | snv | 2.0E-05; 4.0E-06 | 2 | ||
| rs78655421 | 0.716 | 0.240 | 7 | 117530975 | missense variant | G/A;C;T | snv | 1.5E-03; 1.2E-05 | 2 | ||
| rs121908752 | 0.851 | 0.160 | 7 | 117535285 | missense variant | T/G | snv | 1.9E-04 | 1.3E-04 | 2 | |
| rs11971167 | 0.882 | 0.160 | 7 | 117642528 | missense variant | G/A;T | snv | 1.3E-03 | 2 | ||
| 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 |