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 | ||
| rs121908751 | 0.925 | 0.160 | 7 | 117530899 | stop gained | G/A;T | snv | 4.0E-06 | 1 | ||
| rs121908753 | 0.851 | 0.160 | 7 | 117540285 | missense variant | G/A | snv | 2.4E-05 | 1 | ||
| rs121908755 | 0.882 | 0.200 | 7 | 117587800 | missense variant | G/A;T | snv | 8.8E-05 | 1 | ||
| rs121908758 | 0.851 | 0.160 | 7 | 117590394 | missense variant | C/A | snv | 8.0E-06 | 7.0E-06 | 1 | |
| rs121908759 | 0.827 | 0.160 | 7 | 117592032 | missense variant | G/A | snv | 1.0E-04 | 3.8E-04 | 1 | |
| rs121908802 | 0.851 | 0.160 | 7 | 117535263 | missense variant | C/T | snv | 7.0E-06 | 1 | ||
| rs121908803 | 0.925 | 0.160 | 7 | 117535281 | missense variant | C/A;T | snv | 4.0E-06 | 7.0E-06 | 1 | |
| rs121909005 | 0.851 | 0.160 | 7 | 117587801 | missense variant | T/A;C;G | snv | 4.0E-06; 8.0E-06 | 1 | ||
| rs121909006 | 0.925 | 0.160 | 7 | 117590360 | missense variant | T/A;C;G | snv | 8.0E-06 | 1 | ||
| rs121909008 | 0.925 | 0.160 | 7 | 117603612 | missense variant | A/G | snv | 4.0E-06 | 7.0E-06 | 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 | |||
| rs121909019 | 0.925 | 0.160 | 7 | 117611638 | missense variant | G/A;T | snv | 3.2E-05 | 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 | ||
| rs121909036 | 0.925 | 0.160 | 7 | 117611635 | missense variant | T/C;G | snv | 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 |