| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs145848414 | 1.000 | 0.080 | 5 | 174587111 | intergenic variant | G/A | snv | 1.2E-02 | 1 | ||
| rs146446983 | 1.000 | 0.080 | 17 | 31761101 | non coding transcript exon variant | G/A;C | snv | 1 | |||
| rs1466435 | 1.000 | 0.080 | 19 | 44839558 | regulatory region variant | G/C | snv | 7.0E-02 | 1 | ||
| rs146650065 | 1.000 | 0.080 | 10 | 29940940 | intergenic variant | A/G | snv | 5.5E-03 | 1 | ||
| rs147213018 | 1.000 | 0.080 | 9 | 77060964 | intergenic variant | G/A | snv | 5.8E-02 | 1 | ||
| rs147338646 | 1.000 | 0.080 | 9 | 11812813 | intron variant | G/A | snv | 1.0E-03 | 1 | ||
| rs147525344 | 1.000 | 0.080 | 20 | 23762403 | intergenic variant | T/C | snv | 1 | |||
| rs147775533 | 1.000 | 0.080 | 20 | 50382958 | intergenic variant | C/A;T | snv | 1 | |||
| rs148471206 | 1.000 | 0.080 | 3 | 22933695 | intergenic variant | C/T | snv | 1.1E-03 | 1 | ||
| rs148601586 | 1.000 | 0.080 | 19 | 44843409 | upstream gene variant | C/G | snv | 6.6E-03 | 1 | ||
| rs148822902 | 1.000 | 0.080 | 2 | 4989398 | intergenic variant | C/G | snv | 2.7E-02 | 1 | ||
| rs149372995 | 1.000 | 0.080 | 7 | 540903 | intergenic variant | A/G | snv | 7.1E-02 | 1 | ||
| rs149464898 | 1.000 | 0.080 | 17 | 80973533 | upstream gene variant | C/T | snv | 2.4E-02 | 1 | ||
| rs1498853 | 1.000 | 0.080 | 3 | 69559956 | downstream gene variant | C/T | snv | 0.73 | 1 | ||
| rs150252171 | 1.000 | 0.080 | 16 | 62536445 | intergenic variant | A/G | snv | 6.9E-03 | 1 | ||
| rs1513625 | 1.000 | 0.080 | 2 | 100698011 | intergenic variant | G/A;T | snv | 1 | |||
| rs1551891 | 1.000 | 0.080 | 19 | 44728555 | upstream gene variant | G/A | snv | 8.1E-02 | 1 | ||
| rs16847609 | 1.000 | 0.080 | 3 | 137931894 | intergenic variant | G/A | snv | 0.12 | 1 | ||
| rs16887604 | 1.000 | 0.080 | 6 | 76439941 | intergenic variant | C/G;T | snv | 1 | |||
| rs17069431 | 1.000 | 0.080 | 6 | 139874946 | intron variant | C/T | snv | 7.6E-02 | 1 | ||
| rs17117083 | 1.000 | 0.080 | 5 | 155190128 | intron variant | C/T | snv | 3.5E-02 | 1 | ||
| rs17639982 | 1.000 | 0.080 | 2 | 176778182 | intron variant | C/A;G;T | snv | 1 | |||
| rs1774093 | 1.000 | 0.080 | 9 | 101884874 | intergenic variant | A/G | snv | 0.12 | 1 | ||
| rs17745409 | 1.000 | 0.080 | 11 | 86101743 | regulatory region variant | A/G | snv | 0.11 | 1 | ||
| rs1786140 | 1.000 | 0.080 | 11 | 60141154 | intergenic variant | T/C | snv | 0.57 | 1 |