| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs35225200 | 1.000 | 0.040 | 4 | 102225731 | intergenic variant | A/C | snv | 5.4E-02 | 5 | ||
| rs4130548 | 1.000 | 0.040 | 1 | 77998184 | intron variant | T/C | snv | 0.25 | 5 | ||
| rs7359397 | 1.000 | 0.040 | 16 | 28874338 | upstream gene variant | C/T | snv | 0.28 | 5 | ||
| rs12764899 | 1.000 | 0.040 | 10 | 102875346 | intron variant | G/A | snv | 0.21 | 4 | ||
| rs4129585 | 1.000 | 0.040 | 8 | 142231572 | intron variant | A/C | snv | 0.68 | 4 | ||
| rs6704768 | 1.000 | 0.040 | 2 | 232727791 | intron variant | G/A | snv | 0.54 | 4 | ||
| rs6855246 | 1.000 | 0.040 | 4 | 102191313 | intergenic variant | A/G | snv | 0.14 | 4 | ||
| rs10752262 | 1.000 | 0.040 | 10 | 12353101 | intron variant | C/T | snv | 0.39 | 3 | ||
| rs11055980 | 1.000 | 0.040 | 12 | 14458588 | intron variant | C/T | snv | 0.40 | 3 | ||
| rs11210892 | 1.000 | 0.040 | 1 | 43634413 | intergenic variant | G/A | snv | 0.51 | 3 | ||
| rs11740474 | 1.000 | 0.040 | 5 | 154301187 | intron variant | A/T | snv | 0.37 | 3 | ||
| rs11765189 | 1.000 | 0.040 | 7 | 157743285 | intron variant | A/G | snv | 0.25 | 3 | ||
| rs12061601 | 1.000 | 0.040 | 1 | 169101212 | intron variant | T/C | snv | 0.16 | 3 | ||
| rs12443170 | 1.000 | 0.040 | 15 | 78615394 | intron variant | G/A | snv | 0.12 | 3 | ||
| rs12561919 | 1.000 | 0.040 | 1 | 11779866 | missense variant | C/T | snv | 0.13 | 0.13 | 3 | |
| rs12602286 | 1.000 | 0.040 | 17 | 19333641 | intron variant | G/T | snv | 0.79 | 3 | ||
| rs12704290 | 1.000 | 0.040 | 7 | 86798310 | intron variant | G/A | snv | 8.9E-02 | 3 | ||
| rs12826178 | 1.000 | 0.040 | 12 | 57228588 | upstream gene variant | G/T | snv | 5.3E-02 | 3 | ||
| rs133047 | 1.000 | 0.040 | 22 | 40631815 | intron variant | T/C | snv | 0.93 | 3 | ||
| rs1408579 | 1.000 | 0.040 | 10 | 100152437 | intron variant | C/T | snv | 0.32 | 3 | ||
| rs169738 | 1.000 | 0.040 | 6 | 33569769 | intron variant | A/G;T | snv | 3 | |||
| rs1975802 | 1.000 | 0.040 | 16 | 68251944 | intron variant | A/C;G | snv | 3 | |||
| rs2070016 | 1.000 | 0.040 | 4 | 154589162 | intron variant | A/G | snv | 0.12 | 3 | ||
| rs253 | 1.000 | 0.040 | 8 | 19953906 | intron variant | C/T | snv | 0.53 | 3 | ||
| rs2535627 | 1.000 | 0.040 | 3 | 52811089 | downstream gene variant | T/A;C;G | snv | 3 |