| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs121908047 | 0.851 | 0.120 | 1 | 23798188 | missense variant | C/T | snv | 8.0E-06 | 1.4E-05 | 4 | |
| rs137853859 | 0.882 | 0.120 | 1 | 23797718 | missense variant | G/A;T | snv | 7.2E-05; 8.0E-06 | 3 | ||
| rs137853860 | 0.882 | 0.120 | 1 | 23796777 | missense variant | G/A | snv | 1.6E-05 | 7.0E-06 | 3 | |
| rs137853861 | 0.882 | 0.120 | 1 | 23796234 | missense variant | C/T | snv | 2.0E-05 | 3 | ||
| rs28940882 | 0.882 | 0.120 | 1 | 23798199 | missense variant | C/T | snv | 3 | |||
| rs28940884 | 0.882 | 0.120 | 1 | 23796722 | missense variant | T/C | snv | 1.4E-03 | 5.8E-03 | 3 | |
| rs3180383 | 0.882 | 0.120 | 1 | 23796202 | missense variant | G/A;T | snv | 3 | |||
| rs368637540 | 0.882 | 0.120 | 1 | 23795992 | missense variant | C/G;T | snv | 1.2E-05 | 3 | ||
| rs28940885 | 0.925 | 0.120 | 1 | 23796183 | missense variant | C/T | snv | 3.5E-04 | 1.2E-03 | 2 | |
| rs121908045 | 1.000 | 0.120 | 1 | 23797128 | missense variant | A/G | snv | 4.1E-06 | 1 | ||
| rs121908046 | 1.000 | 0.120 | 1 | 23798907 | missense variant | T/C | snv | 2.0E-05; 4.0E-06 | 7.0E-06 | 1 | |
| rs1261697960 | 1.000 | 0.120 | 1 | 23798645 | missense variant | G/T | snv | 4.0E-06 | 1 | ||
| rs1431772923 | 1.000 | 0.120 | 1 | 23798934 | missense variant | G/A | snv | 4.0E-06 | 1 | ||
| rs144492228 | 1.000 | 0.120 | 1 | 23798890 | missense variant | G/A;T | snv | 1.6E-05; 4.0E-06 | 1 | ||
| rs28940883 | 1.000 | 0.120 | 1 | 23798160 | missense variant | T/C | snv | 4.0E-06 | 1 | ||
| rs528467258 | 1.000 | 0.120 | 1 | 23797730 | missense variant | C/T | snv | 4.0E-06 | 1 |