| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs6734238 | 1.000 | 0.080 | 2 | 113083453 | upstream gene variant | A/G | snv | 0.39 | 8 | ||
| rs2067087 | 1.000 | 0.080 | 7 | 27202041 | non coding transcript exon variant | G/C;T | snv | 6 | |||
| rs10203853 | 1.000 | 0.080 | 2 | 233778772 | intron variant | A/G;T | snv | 5 | |||
| rs10929251 | 1.000 | 0.080 | 2 | 233637583 | intron variant | A/G | snv | 0.13 | 5 | ||
| rs17864678 | 1.000 | 0.080 | 2 | 233635964 | intron variant | T/A | snv | 5.6E-03 | 5 | ||
| rs6728940 | 1.000 | 0.080 | 2 | 233780518 | intron variant | G/A | snv | 0.26 | 5 | ||
| rs1044471 | 1.000 | 0.080 | 12 | 1787790 | 3 prime UTR variant | C/T | snv | 0.38 | 4 | ||
| rs2302427 | 1.000 | 0.080 | 7 | 148828812 | missense variant | C/G | snv | 7.8E-02 | 6.0E-02 | 4 | |
| rs4642 | 1.000 | 0.080 | 17 | 47292411 | synonymous variant | A/G | snv | 0.29 | 0.29 | 4 | |
| rs1133683 | 1.000 | 0.080 | 17 | 65537650 | synonymous variant | G/A | snv | 0.60; 5.4E-06 | 0.53 | 3 | |
| rs1196644309 | 1.000 | 0.080 | 1 | 145995155 | missense variant | G/A | snv | 3 | |||
| rs12881063 | 1.000 | 0.080 | 14 | 20788017 | downstream gene variant | G/C | snv | 7.4E-02 | 3 | ||
| rs1500482 | 1.000 | 0.080 | 2 | 233774392 | upstream gene variant | C/A;T | snv | 3 | |||
| rs199734815 | 1.000 | 0.080 | 10 | 129708022 | missense variant | C/T | snv | 6.0E-05 | 3 | ||
| rs2735970 | 1.000 | 0.080 | 11 | 2000585 | intron variant | T/C | snv | 3 | |||
| rs34374438 | 1.000 | 0.080 | 2 | 47800544 | missense variant | A/T | snv | 3.9E-04 | 3.5E-04 | 3 | |
| rs3764482 | 1.000 | 0.080 | 18 | 48942576 | non coding transcript exon variant | G/A | snv | 0.14 | 0.13 | 3 | |
| rs61926301 | 1.000 | 0.080 | 12 | 50764080 | 5 prime UTR variant | G/C;T | snv | 3 | |||
| rs7586006 | 1.000 | 0.080 | 2 | 233776881 | intron variant | T/A;G | snv | 3 | |||
| rs763693540 | 1.000 | 0.080 | 1 | 45333573 | missense variant | C/A;T | snv | 4.0E-06; 4.0E-06 | 3 | ||
| rs765388668 | 1.000 | 0.080 | 7 | 92002488 | missense variant | T/A | snv | 8.1E-06 | 3 | ||
| rs7959129 | 1.000 | 0.080 | 12 | 50775325 | intron variant | T/G | snv | 0.84 | 3 | ||
| rs1040264140 | 1.000 | 0.080 | 15 | 90881744 | missense variant | A/G | snv | 2 | |||
| rs1057519739 | 1.000 | 0.080 | 18 | 51065518 | missense variant | G/A;C | snv | 2 | |||
| rs10929732 | 1.000 | 0.080 | 2 | 11343366 | intron variant | A/G | snv | 0.72 | 2 |