| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs2055729 | 1.000 | 0.160 | 8 | 9935152 | intergenic variant | G/A | snv | 0.54 | 1 | ||
| rs28801070 | 1.000 | 0.160 | 2 | 185380090 | intergenic variant | G/A | snv | 1 | |||
| rs34101942 | 1.000 | 0.160 | 22 | 39167907 | intergenic variant | -/A | delins | 0.68 | 1 | ||
| rs34229995 | 1.000 | 0.160 | 6 | 15243787 | upstream gene variant | C/G | snv | 2.1E-02 | 1 | ||
| rs56332587 | 1.000 | 0.160 | 3 | 41971222 | intergenic variant | T/C | snv | 0.12 | 1 | ||
| rs58916656 | 1.000 | 0.160 | 3 | 41971289 | intergenic variant | C/G | snv | 0.12 | 1 | ||
| rs6071887 | 1.000 | 0.160 | 20 | 39992814 | intergenic variant | A/G;T | snv | 1 | |||
| rs73073229 | 1.000 | 0.160 | 3 | 41966358 | upstream gene variant | T/C | snv | 0.12 | 1 | ||
| rs73073230 | 1.000 | 0.160 | 3 | 41966771 | upstream gene variant | G/A;C | snv | 1 | |||
| rs73073233 | 1.000 | 0.160 | 3 | 41969058 | intergenic variant | A/G | snv | 0.12 | 1 | ||
| rs73073234 | 1.000 | 0.160 | 3 | 41970579 | intergenic variant | C/T | snv | 0.12 | 1 | ||
| rs73073235 | 1.000 | 0.160 | 3 | 41971201 | intergenic variant | C/A;T | snv | 0.12 | 1 | ||
| rs73073238 | 1.000 | 0.160 | 3 | 41972833 | upstream gene variant | G/C | snv | 0.12 | 1 | ||
| rs7373694 | 1.000 | 0.160 | 3 | 41971227 | intergenic variant | G/A | snv | 0.68 | 1 | ||
| rs74947509 | 1.000 | 0.160 | 3 | 41964831 | upstream gene variant | T/C | snv | 0.14 | 1 | ||
| rs7629767 | 1.000 | 0.160 | 3 | 42002017 | intergenic variant | T/G | snv | 0.16 | 1 | ||
| rs7634985 | 1.000 | 0.160 | 3 | 41978073 | downstream gene variant | C/T | snv | 0.72 | 1 | ||
| rs78629637 | 1.000 | 0.160 | 3 | 41967289 | intergenic variant | C/A;T | snv | 1 | |||
| rs794894 | 1.000 | 0.160 | 3 | 41990991 | intergenic variant | C/T | snv | 0.74 | 1 | ||
| rs9835059 | 1.000 | 0.160 | 3 | 41968234 | intergenic variant | A/G;T | snv | 1 | |||
| rs1045642 | 0.456 | 0.840 | 7 | 87509329 | synonymous variant | A/G;T | snv | 0.50 | 214 | ||
| rs2032582 | 0.538 | 0.800 | 7 | 87531302 | missense variant | A/C;T | snv | 0.54; 3.8E-02 | 97 | ||
| rs1128503 | 0.564 | 0.760 | 7 | 87550285 | synonymous variant | A/G | snv | 0.54 | 0.63 | 64 | |
| rs1289543302 | 0.763 | 0.440 | 7 | 87536472 | missense variant | C/T | snv | 12 | |||
| rs4148388 | 1.000 | 0.160 | 10 | 99790008 | intron variant | G/A;C | snv | 1 |