Source: UNIPROT
| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs1177201180 | 1.000 | 0.120 | 7 | 117592160 | missense variant | A/T | snv | 1 | |||
| rs121908750 | 1.000 | 0.120 | 7 | 117509140 | missense variant | G/A | snv | 4.0E-06 | 1 | ||
| rs121909009 | 1.000 | 0.120 | 7 | 117548804 | missense variant | G/T | snv | 1 | |||
| rs121909013 | 1.000 | 0.120 | 7 | 117587805 | missense variant | G/A | snv | 4.0E-06 | 1 | ||
| rs121909015 | 1.000 | 0.120 | 7 | 117642593 | missense variant | G/C | snv | 8.0E-06 | 1 | ||
| rs121909016 | 1.000 | 0.120 | 7 | 117540163 | missense variant | C/G | snv | 1 | |||
| rs121909020 | 1.000 | 0.120 | 7 | 117611640 | missense variant | G/A;C | snv | 4.0E-06 | 1 | ||
| rs121909028 | 1.000 | 0.120 | 7 | 117642577 | missense variant | T/C | snv | 1 | |||
| rs121909031 | 1.000 | 0.120 | 7 | 117530951 | missense variant | A/G | snv | 1 | |||
| rs121909033 | 1.000 | 0.120 | 7 | 117592110 | missense variant | A/T | snv | 1 | |||
| rs121909035 | 1.000 | 0.120 | 7 | 117603719 | missense variant | C/T | snv | 4.0E-06 | 1 | ||
| rs121909037 | 1.000 | 0.120 | 7 | 117611653 | missense variant | A/C;G | snv | 4.0E-06 | 1 | ||
| rs121909040 | 1.000 | 0.120 | 7 | 117642466 | missense variant | G/A | snv | 7.0E-06 | 1 | ||
| rs121909041 | 1.000 | 0.120 | 7 | 117642483 | missense variant | T/A;C | snv | 4.0E-06 | 1 | ||
| rs121909042 | 1.000 | 0.120 | 7 | 117652875 | missense variant | A/C;T | snv | 4.0E-06 | 1 | ||
| rs143456784 | 1.000 | 0.120 | 7 | 117504324 | missense variant | C/T | snv | 1.2E-04 | 7.7E-05 | 1 | |
| rs143486492 | 1.000 | 0.120 | 7 | 117540120 | missense variant | G/A | snv | 5.7E-04 | 5.7E-04 | 1 | |
| rs145540754 | 1.000 | 0.120 | 7 | 117592246 | missense variant | T/G | snv | 7.2E-05; 8.0E-06 | 3.1E-04 | 1 | |
| rs149353983 | 1.000 | 0.120 | 7 | 117504291 | missense variant | G/A;T | snv | 5.6E-05; 3.2E-05 | 1 | ||
| rs150157202 | 0.925 | 0.120 | 7 | 117592427 | missense variant | G/A;T | snv | 1.8E-03 | 1.7E-03 | 1 | |
| rs150212784 | 1.000 | 0.120 | 7 | 117611595 | missense variant | T/C;G | snv | 4.0E-06; 6.5E-04 | 1 | ||
| rs150691494 | 1.000 | 0.120 | 7 | 117540132 | missense variant | A/G | snv | 2.9E-04 | 1.8E-04 | 1 | |
| rs1800074 | 1.000 | 0.120 | 7 | 117504330 | missense variant | A/G;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 | |
| rs193922506 | 1.000 | 0.120 | 7 | 117595036 | missense variant | G/A | snv | 4.8E-05 | 4.9E-05 | 1 |