| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs1555902 | 1.000 | 0.160 | 13 | 108204435 | downstream gene variant | C/A | snv | 0.10 | 1 | ||
| rs193451 | 1.000 | 0.160 | 7 | 108670542 | intergenic variant | A/G | snv | 0.36 | 1 | ||
| rs79480871 | 0.925 | 0.160 | 2 | 24471603 | intergenic variant | C/T | snv | 9.3E-02 | 1 | ||
| rs4148388 | 1.000 | 0.160 | 10 | 99790008 | intron variant | G/A;C | snv | 1 | |||
| rs1450703683 | 1.000 | 0.160 | X | 8533018 | missense variant | T/C | snv | 1.9E-05 | 1 | ||
| rs1057519718 | 0.925 | 0.160 | 7 | 140753355 | missense variant | CA/TC | mnv | 1 | |||
| rs397516896 | 0.763 | 0.360 | 7 | 140753355 | missense variant | C/G;T | snv | 1 | |||
| rs1250801605 | 1.000 | 0.160 | 2 | 201185809 | missense variant | G/A | snv | 4.0E-06 | 1 | ||
| rs559979934 | 1.000 | 0.160 | 2 | 201185838 | missense variant | C/G;T | snv | 4.8E-05 | 2.1E-05 | 1 | |
| rs145738773 | 1.000 | 0.160 | 1 | 15504663 | synonymous variant | G/A | snv | 4.4E-05 | 1.0E-04 | 1 | |
| rs710190 | 0.925 | 0.200 | 22 | 39131785 | 3 prime UTR variant | T/C | snv | 0.48 | 1 | ||
| rs877529 | 1.000 | 0.160 | 22 | 39146287 | intron variant | G/A | snv | 0.43 | 1 | ||
| rs11064392 | 1.000 | 0.160 | 12 | 6789226 | intron variant | A/G | snv | 0.14 | 1 | ||
| rs104894340 | 0.827 | 0.200 | 12 | 57751647 | missense variant | C/A;T | snv | 1 | |||
| rs711613 | 1.000 | 0.160 | 3 | 3178805 | intron variant | T/C | snv | 0.51 | 1 | ||
| rs143267032 | 1.000 | 0.160 | 7 | 102028117 | missense variant | C/G | snv | 2.8E-05 | 2.8E-05 | 1 | |
| rs1049633 | 1.000 | 0.160 | 6 | 30899750 | 3 prime UTR variant | G/A | snv | 7.6E-02 | 1 | ||
| rs6746082 | 1.000 | 0.160 | 2 | 25436375 | intron variant | A/C;T | snv | 1 | |||
| rs3777189 | 1.000 | 0.160 | 5 | 95917404 | intron variant | C/G | snv | 0.34 | 1 | ||
| rs3815768 | 1.000 | 0.160 | 5 | 95900755 | missense variant | C/T | snv | 0.27 | 0.29 | 1 | |
| rs777103792 | 1.000 | 0.160 | 8 | 38419678 | missense variant | T/C | snv | 1.2E-05 | 2.1E-05 | 1 | |
| rs72773978 | 1.000 | 0.160 | 16 | 15880785 | intron variant | A/T | snv | 8.1E-02 | 1 | ||
| rs210143 | 0.827 | 0.160 | 6 | 33579153 | intron variant | T/C | snv | 0.74 | 1 | ||
| rs121917759 | 0.790 | 0.480 | 11 | 533466 | missense variant | G/A | snv | 1 | |||
| rs765506701 | 1.000 | 0.160 | 21 | 33288130 | missense variant | G/A;C | snv | 4.0E-06; 8.0E-06 | 1 |