| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs2189234 | 1.000 | 0.040 | 4 | 105154341 | intron variant | T/G | snv | 0.62 | 3 | ||
| rs2382817 | 0.925 | 0.040 | 2 | 218286495 | 5 prime UTR variant | A/C | snv | 0.61 | 3 | ||
| rs2395128 | 1.000 | 0.040 | 10 | 75052692 | intron variant | G/T | snv | 0.32 | 2 | ||
| rs2413583 | 0.925 | 0.040 | 22 | 39263768 | intron variant | C/T | snv | 0.19 | 3 | ||
| rs2488389 | 0.925 | 0.040 | 1 | 197662011 | intron variant | G/A | snv | 0.22 | 3 | ||
| rs254560 | 1.000 | 0.040 | 5 | 135107916 | intron variant | G/A | snv | 0.32 | 2 | ||
| rs2651244 | 1.000 | 0.040 | 1 | 70529879 | upstream gene variant | G/A | snv | 0.30 | 2 | ||
| rs2823286 | 0.925 | 0.040 | 21 | 15445619 | intron variant | G/A | snv | 0.28 | 3 | ||
| rs2930047 | 0.925 | 0.040 | 5 | 10695414 | intron variant | T/C | snv | 0.49 | 3 | ||
| rs35675666 | 1.000 | 0.040 | 1 | 7961913 | 5 prime UTR variant | G/C;T | snv | 2 | |||
| rs3742130 | 0.925 | 0.040 | 13 | 99255087 | synonymous variant | G/A | snv | 0.16 | 0.16 | 3 | |
| rs3851228 | 0.925 | 0.040 | 6 | 111526988 | intron variant | A/T | snv | 9.7E-02 | 3 | ||
| rs4380874 | 1.000 | 0.040 | 7 | 107839870 | intergenic variant | T/A;C;G | snv | 2 | |||
| rs4409764 | 0.925 | 0.040 | 10 | 99524480 | upstream gene variant | T/A;G | snv | 3 | |||
| rs4656958 | 0.925 | 0.040 | 1 | 160887174 | upstream gene variant | A/G;T | snv | 3 | |||
| rs4676408 | 1.000 | 0.040 | 2 | 240634984 | downstream gene variant | G/A;T | snv | 0.57 | 2 | ||
| rs4743820 | 1.000 | 0.040 | 9 | 91166134 | non coding transcript exon variant | C/T | snv | 0.61 | 2 | ||
| rs483905 | 1.000 | 0.040 | 11 | 96290263 | intron variant | G/A | snv | 0.26 | 2 | ||
| rs501916 | 1.000 | 0.040 | 15 | 47761032 | synonymous variant | C/A | snv | 0.40 | 0.41 | 2 | |
| rs561722 | 1.000 | 0.040 | 11 | 114516108 | upstream gene variant | C/T | snv | 0.35 | 2 | ||
| rs5763767 | 0.925 | 0.040 | 22 | 30097893 | intron variant | G/A;T | snv | 3 | |||
| rs6062504 | 0.925 | 0.040 | 20 | 63717555 | intron variant | A/G;T | snv | 3 | |||
| rs6667605 | 1.000 | 0.040 | 1 | 2571341 | downstream gene variant | C/T | snv | 0.53 | 3 | ||
| rs6740847 | 0.925 | 0.040 | 2 | 181443625 | intergenic variant | A/G | snv | 0.57 | 8 | ||
| rs6927022 | 1.000 | 0.040 | 6 | 32644620 | non coding transcript exon variant | A/G | snv | 0.42 | 2 |