| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs776746 | 0.724 | 0.400 | 7 | 99672916 | splice acceptor variant | T/C | snv | 0.72 | 21 | ||
| rs1474798132 | 0.925 | 0.120 | 7 | 99665170 | synonymous variant | T/A;C | snv | 4.0E-06; 4.0E-06 | 2 | ||
| rs17525495 | 0.882 | 0.080 | 12 | 96035599 | 5 prime UTR variant | G/A | snv | 9.9E-02 | 4 | ||
| rs3742330 | 0.662 | 0.640 | 14 | 95087025 | 3 prime UTR variant | A/G | snv | 8.7E-02 | 24 | ||
| rs4986893 | 0.827 | 0.240 | 10 | 94780653 | stop gained | G/A | snv | 5.4E-03 | 1.5E-03 | 5 | |
| rs39509 | 1.000 | 0.040 | 8 | 89791937 | downstream gene variant | G/A | snv | 0.65 | 1 | ||
| rs218916 | 1.000 | 0.040 | 8 | 89688709 | intron variant | C/T | snv | 0.67 | 2 | ||
| rs160441 | 1.000 | 0.040 | 8 | 89644760 | intron variant | T/C | snv | 0.55 | 2 | ||
| rs3794624 | 0.882 | 0.120 | 16 | 88650666 | intron variant | G/A | snv | 0.26 | 0.29 | 4 | |
| rs1128503 | 0.564 | 0.760 | 7 | 87550285 | synonymous variant | A/G | snv | 0.54 | 0.63 | 64 | |
| rs2032582 | 0.538 | 0.800 | 7 | 87531302 | missense variant | A/C;T | snv | 0.54; 3.8E-02 | 97 | ||
| rs1045642 | 0.456 | 0.840 | 7 | 87509329 | synonymous variant | A/G;T | snv | 0.50 | 214 | ||
| rs80292941 | 1.000 | 0.040 | 2 | 87480257 | non coding transcript exon variant | A/T | snv | 0.16 | 2 | ||
| rs10514611 | 0.925 | 0.080 | 16 | 85921636 | 3 prime UTR variant | C/T | snv | 0.23 | 2 | ||
| rs11117415 | 1.000 | 0.040 | 16 | 85917080 | intron variant | A/G | snv | 0.12 | 1 | ||
| rs925994 | 0.925 | 0.080 | 16 | 85912411 | intron variant | C/A | snv | 6.7E-02 | 2 | ||
| rs534448891 | 1.000 | 0.040 | 16 | 85413567 | intron variant | C/G;T | snv | 6.3E-05 | 1 | ||
| rs11040 | 1.000 | 0.040 | 6 | 81752132 | missense variant | C/A;G;T | snv | 1 | |||
| rs1059225 | 1.000 | 0.040 | 10 | 79615230 | 3 prime UTR variant | T/C | snv | 0.47 | 1 | ||
| rs1914663 | 1.000 | 0.040 | 10 | 79612197 | intron variant | C/T | snv | 0.11 | 1 | ||
| rs1650232 | 1.000 | 0.040 | 10 | 79559511 | splice region variant | C/A;T | snv | 3.6E-03; 0.71 | 2 | ||
| rs17879335 | 1.000 | 0.040 | 10 | 79556699 | 3 prime UTR variant | C/A | snv | 0.38 | 1 | ||
| rs17881720 | 1.000 | 0.040 | 10 | 79555670 | downstream gene variant | T/C | snv | 6.7E-02 | 1 | ||
| rs4842407 | 0.882 | 0.200 | 12 | 78807293 | intron variant | A/G | snv | 0.35 | 4 | ||
| rs8064821 | 0.851 | 0.120 | 17 | 78361310 | intron variant | C/A | snv | 0.17 | 6 |