Source: CURATED
| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs1057521085 | 1.000 | 0.080 | 1 | 21561142 | missense variant | A/G | snv | 7.0E-06 | 1 | ||
| rs1159854007 | 1.000 | 0.080 | 1 | 21563194 | missense variant | G/A | snv | 7.0E-06 | 1 | ||
| rs1196976671 | 1.000 | 0.080 | 1 | 21577475 | missense variant | G/A | snv | 7.0E-06 | 1 | ||
| rs121918012 | 1.000 | 0.080 | 1 | 21564053 | missense variant | G/T | snv | 1 | |||
| rs1220125702 | 1.000 | 0.080 | 1 | 21573686 | missense variant | T/C | snv | 8.0E-06 | 7.0E-06 | 1 | |
| rs1223142821 | 1.000 | 0.080 | 1 | 21568193 | missense variant | G/T | snv | 4.0E-06 | 1 | ||
| rs1304394441 | 1.000 | 0.080 | 1 | 21561138 | missense variant | G/A | snv | 1 | |||
| rs1376937780 | 1.000 | 0.080 | 1 | 21563255 | missense variant | C/T | snv | 1 | |||
| rs138690664 | 0.851 | 0.120 | 1 | 21577421 | missense variant | C/G;T | snv | 1.6E-05 | 3.5E-05 | 1 | |
| rs1470389268 | 1.000 | 0.080 | 1 | 21560716 | missense variant | C/T | snv | 4.0E-06 | 7.0E-06 | 1 | |
| rs149344982 | 1.000 | 0.080 | 1 | 21563267 | missense variant | G/A | snv | 1.2E-02 | 8.6E-03 | 1 | |
| rs150799088 | 0.925 | 0.080 | 1 | 21577422 | missense variant | G/A | snv | 7.7E-05 | 7.0E-06 | 1 | |
| rs1553414079 | 1.000 | 0.080 | 1 | 21573682 | missense variant | G/T | snv | 1 | |||
| rs1553414563 | 1.000 | 0.080 | 1 | 21575777 | missense variant | G/A | snv | 1 | |||
| rs1553414568 | 1.000 | 0.080 | 1 | 21575797 | missense variant | G/C | snv | 1 | |||
| rs1553415041 | 1.000 | 0.080 | 1 | 21577406 | missense variant | T/C | snv | 1 | |||
| rs760029254 | 1.000 | 0.080 | 1 | 21564052 | missense variant | G/A | snv | 1.6E-05 | 1 | ||
| rs763457259 | 1.000 | 0.080 | 1 | 21573733 | missense variant | G/A | snv | 7.0E-06 | 1 | ||
| rs765458125 | 1.000 | 0.080 | 1 | 21573676 | missense variant | C/A;T | snv | 8.0E-06; 4.0E-06 | 1 | ||
| rs770093969 | 1.000 | 0.080 | 1 | 21560683 | missense variant | C/G;T | snv | 4.0E-06; 1.2E-05 | 1 | ||
| rs773257111 | 1.000 | 0.080 | 1 | 21563143 | missense variant | G/A | snv | 8.0E-06 | 7.0E-06 | 1 | |
| rs778232217 | 1.000 | 0.080 | 1 | 21564080 | missense variant | A/G | snv | 8.0E-06 | 1 | ||
| rs780583917 | 1.000 | 0.080 | 1 | 21563213 | missense variant | C/A | snv | 5.2E-05 | 6.3E-05 | 1 | |
| rs954135116 | 1.000 | 0.080 | 1 | 21563170 | missense variant | G/A | snv | 4.0E-06 | 1 | ||
| rs966212736 | 1.000 | 0.080 | 1 | 21577427 | missense variant | G/A | snv | 7.0E-06 | 1 |