| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs1001684 | 1.000 | 0.040 | 5 | 40810324 | intergenic variant | C/A | snv | 0.29 | 1 | ||
| rs1002424 | 1.000 | 0.040 | 5 | 40767295 | intron variant | A/G | snv | 0.31 | 1 | ||
| rs10065570 | 1.000 | 0.040 | 5 | 40835525 | upstream gene variant | C/T | snv | 0.33 | 1 | ||
| rs1006737 | 0.695 | 0.120 | 12 | 2236129 | intron variant | G/A | snv | 0.36 | 6 | ||
| rs10074991 | 0.851 | 0.120 | 5 | 40790449 | intron variant | G/A | snv | 0.31 | 1 | ||
| rs10135277 | 1.000 | 0.040 | 14 | 35354025 | TF binding site variant | C/T | snv | 0.43 | 1 | ||
| rs10140896 | 1.000 | 0.040 | 14 | 88752194 | intron variant | C/A;G;T | snv | 1 | |||
| rs10155413 | 1.000 | 0.040 | 4 | 137116128 | intron variant | T/C | snv | 0.35 | 1 | ||
| rs10226475 | 1.000 | 0.040 | 7 | 2186527 | intron variant | A/G | snv | 0.34 | 1 | ||
| rs1025641 | 1.000 | 0.040 | 10 | 126618623 | intron variant | T/C | snv | 0.43 | 1 | ||
| rs10275045 | 0.882 | 0.160 | 7 | 1881190 | intron variant | C/T | snv | 0.35 | 3 | ||
| rs1035130 | 1.000 | 0.040 | 2 | 102384942 | synonymous variant | C/T | snv | 0.26 | 0.24 | 1 | |
| rs10423928 | 0.807 | 0.200 | 19 | 45679046 | intron variant | T/A | snv | 0.19 | 2 | ||
| rs1042779 | 0.882 | 0.040 | 3 | 52786995 | missense variant | A/G | snv | 0.40 | 0.42 | 2 | |
| rs10429924 | 1.000 | 0.040 | 1 | 244227262 | intergenic variant | C/T | snv | 8.8E-02 | 1 | ||
| rs1046778 | 0.851 | 0.160 | 10 | 102901727 | 3 prime UTR variant | T/C | snv | 0.30 | 1 | ||
| rs10484399 | 0.851 | 0.240 | 6 | 27566749 | intergenic variant | A/G | snv | 5.4E-02 | 3 | ||
| rs10489202 | 0.925 | 0.080 | 1 | 167933841 | intron variant | G/T | snv | 0.20 | 1 | ||
| rs10498146 | 1.000 | 0.040 | 2 | 222987318 | intergenic variant | A/G | snv | 6.2E-02 | 1 | ||
| rs10503253 | 0.851 | 0.040 | 8 | 4323322 | intron variant | C/A | snv | 0.18 | 2 | ||
| rs10503256 | 1.000 | 0.040 | 8 | 4356657 | intron variant | A/G | snv | 0.57 | 1 | ||
| rs10503899 | 1.000 | 0.040 | 8 | 32089718 | intron variant | A/G | snv | 0.33 | 1 | ||
| rs1051730 | 0.641 | 0.600 | 15 | 78601997 | synonymous variant | G/A | snv | 0.27 | 0.26 | 7 | |
| rs1055569 | 0.882 | 0.240 | 6 | 31472305 | non coding transcript exon variant | C/T | snv | 0.41 | 2 | ||
| rs1061170 | 0.561 | 0.720 | 1 | 196690107 | missense variant | C/T | snv | 0.68 | 0.64 | 1 |