| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs11216943 | 1.000 | 0.040 | 11 | 118685689 | downstream gene variant | G/A | snv | 0.20 | 1 | ||
| rs147061479 | 1.000 | 0.040 | 8 | 65264756 | intergenic variant | C/T | snv | 1.9E-02 | 1 | ||
| rs6554759 | 1.000 | 0.040 | 5 | 1316987 | downstream gene variant | G/A | snv | 0.85 | 1 | ||
| rs7300686 | 1.000 | 0.040 | 12 | 128062664 | intron variant | C/A;T | snv | 1 | |||
| rs9841110 | 1.000 | 0.040 | 3 | 49455048 | regulatory region variant | C/G | snv | 0.28 | 1 | ||
| rs201963 | 1.000 | 0.040 | 8 | 39721376 | intron variant | A/C | snv | 1 | |||
| rs1131239 | 1.000 | 0.040 | 4 | 121696590 | 5 prime UTR variant | G/A;C;T | snv | 0.12 | 0.17 | 1 | |
| rs145619195 | 1.000 | 0.040 | 4 | 121674585 | intron variant | T/C | snv | 9.4E-04 | 1 | ||
| rs2306415 | 1.000 | 0.040 | 4 | 121696476 | intron variant | C/G | snv | 0.16 | 1 | ||
| rs2306420 | 1.000 | 0.040 | 4 | 121670320 | intron variant | G/A | snv | 0.21 | 1 | ||
| rs41278075 | 1.000 | 0.040 | 4 | 121669758 | intron variant | G/A | snv | 0.23 | 0.18 | 1 | |
| rs762541432 | 1.000 | 0.040 | 11 | 27657901 | missense variant | T/C | snv | 4.0E-06 | 1 | ||
| rs12544799 | 1.000 | 0.040 | 8 | 129651264 | intron variant | A/G | snv | 0.34 | 1 | ||
| rs16904140 | 1.000 | 0.040 | 8 | 129653397 | intron variant | G/A | snv | 0.19 | 1 | ||
| rs4636162 | 1.000 | 0.040 | 8 | 129627294 | non coding transcript exon variant | G/A | snv | 0.30 | 1 | ||
| rs6985166 | 1.000 | 0.040 | 8 | 129666930 | intron variant | A/G | snv | 0.34 | 1 | ||
| rs9656979 | 1.000 | 0.040 | 8 | 129652161 | intron variant | T/C | snv | 0.37 | 1 | ||
| rs147960238 | 1.000 | 0.040 | 12 | 7485786 | intron variant | T/C | snv | 8.3E-03 | 1 | ||
| rs1431316232 | 1.000 | 0.040 | 9 | 22006021 | missense variant | A/G | snv | 1 | |||
| rs414965 | 1.000 | 0.040 | 5 | 1324006 | non coding transcript exon variant | G/A | snv | 0.42 | 1 | ||
| rs782414948 | 1.000 | 0.040 | 7 | 102227624 | missense variant | G/A | snv | 3.2E-05 | 2.8E-05 | 1 | |
| rs104894156 | 1.000 | 0.040 | 10 | 122582793 | missense variant | G/T | snv | 1 | |||
| rs1344733 | 1.000 | 0.040 | 2 | 55900892 | intron variant | T/C | snv | 0.41 | 1 | ||
| rs1346786 | 1.000 | 0.040 | 2 | 55881198 | intron variant | C/T | snv | 0.36 | 1 | ||
| rs727878 | 1.000 | 0.040 | 2 | 55892522 | intron variant | C/T | snv | 0.40 | 1 |