| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs1222174664 | 0.827 | 0.280 | 5 | 102477801 | missense variant | G/A | snv | 8.0E-06 | 7.0E-06 | 5 | |
| rs755660650 | 0.827 | 0.120 | 5 | 102498596 | missense variant | G/C | snv | 4.0E-06 | 5 | ||
| rs1417373701 | 0.925 | 0.120 | 5 | 102399606 | missense variant | G/A | snv | 4.0E-06 | 2 | ||
| rs554903493 | 1.000 | 0.120 | 5 | 102419940 | missense variant | G/A | snv | 8.2E-06 | 2 | ||
| rs6878284 | 0.925 | 0.040 | 5 | 102434022 | intron variant | C/T | snv | 0.64 | 2 | ||
| rs773403329 | 0.925 | 0.120 | 5 | 102419925 | missense variant | A/G | snv | 4.1E-06 | 7.0E-06 | 2 | |
| rs7734060 | 0.925 | 0.040 | 5 | 102444775 | intron variant | T/G | snv | 0.19 | 2 | ||
| rs867538330 | 0.925 | 0.080 | 5 | 102458457 | synonymous variant | C/T | snv | 2 | |||
| rs10073892 | 5 | 102391066 | non coding transcript exon variant | T/C | snv | 0.24 | 0.21 | 1 | |||
| rs1255801434 | 1.000 | 0.080 | 5 | 102438650 | missense variant | T/C | snv | 4.3E-06 | 1 | ||
| rs1321703512 | 1.000 | 0.120 | 5 | 102477684 | missense variant | A/G | snv | 1.2E-05 | 1 | ||
| rs1414521156 | 5 | 102459731 | missense variant | T/A;C | snv | 4.0E-06; 4.0E-06 | 1 | ||||
| rs779587631 | 1.000 | 0.080 | 5 | 102438632 | missense variant | C/T | snv | 1 | |||
| rs921877174 | 1.000 | 0.080 | 5 | 102498796 | missense variant | T/C | snv | 1 |