| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs13107325 | 0.776 | 0.520 | 4 | 102267552 | missense variant | C/A;T | snv | 4.0E-06; 4.5E-02 | 24 | ||
| rs143384 | 0.827 | 0.200 | 20 | 35437976 | 5 prime UTR variant | G/A | snv | 0.44 | 13 | ||
| rs2145272 | 20 | 6645571 | intergenic variant | G/A;T | snv | 7 | |||||
| rs1513272 | 7 | 28160478 | intron variant | C/T | snv | 0.40 | 4 | ||||
| rs6780171 | 3 | 185785668 | intron variant | T/A | snv | 0.39 | 4 | ||||
| rs3764002 | 1.000 | 0.080 | 12 | 108224853 | missense variant | C/T | snv | 0.27 | 0.20 | 3 | |
| rs56196860 | 12 | 2799164 | missense variant | C/A | snv | 1.8E-02 | 2.0E-02 | 3 | |||
| rs61823192 | 1 | 219121228 | intron variant | C/T | snv | 1.6E-02 | 3 | ||||
| rs17764730 | 5 | 128021834 | non coding transcript exon variant | C/T | snv | 0.17 | 2 | ||||
| rs2236519 | 20 | 46900932 | intron variant | G/A;T | snv | 2 | |||||
| rs4722530 | 7 | 25844482 | regulatory region variant | G/T | snv | 0.24 | 2 |