| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs3740066 | 0.724 | 0.440 | 10 | 99844450 | missense variant | C/G;T | snv | 2.4E-05; 0.34 | 20 | ||
| rs2273697 | 0.776 | 0.360 | 10 | 99804058 | missense variant | G/A | snv | 0.19 | 0.19 | 11 | |
| rs717620 | 0.763 | 0.240 | 10 | 99782821 | 5 prime UTR variant | C/T | snv | 0.17 | 0.15 | 10 | |
| rs8187710 | 0.827 | 0.200 | 10 | 99851537 | missense variant | G/A | snv | 5.3E-02 | 8.5E-02 | 6 | |
| rs1382048442 | 0.925 | 0.160 | 10 | 99797141 | missense variant | T/C | snv | 4.0E-06 | 2 | ||
| rs4148396 | 0.925 | 0.040 | 10 | 99832187 | intron variant | T/C | snv | 0.65 | 2 | ||
| rs1885301 | 0.925 | 0.040 | 10 | 99781296 | upstream gene variant | A/G | snv | 0.58 | 2 | ||
| rs17222723 | 0.925 | 0.080 | 10 | 99836239 | missense variant | T/A | snv | 4.5E-02 | 5.5E-02 | 2 | |
| rs3740071 | 10 | 99830363 | missense variant | G/A;C | snv | 4.0E-06; 4.0E-06 | 1 | ||||
| rs776087856 | 1.000 | 0.040 | 10 | 99804134 | stop gained | G/A | snv | 4.0E-06 | 1 | ||
| rs72558201 | 1.000 | 0.080 | 10 | 99836193 | missense variant | A/G;T | snv | 4.0E-06; 3.6E-05 | 1 | ||
| rs72558202 | 1.000 | 0.080 | 10 | 99845781 | missense variant | A/G | snv | 7.0E-06 | 1 | ||
| rs56199535 | 1.000 | 0.080 | 10 | 99818820 | missense variant | C/A;G;T | snv | 8.8E-05 | 1 | ||
| rs371866713 | 1.000 | 0.080 | 10 | 99799313 | stop gained | C/A;G | snv | 4.0E-06; 2.8E-05 | 1.0E-04 | 1 | |
| rs72558200 | 1.000 | 0.080 | 10 | 99836125 | missense variant | G/A | snv | 9.1E-05 | 8.4E-05 | 1 | |
| rs1226153645 | 1.000 | 0.080 | 10 | 99813076 | missense variant | G/C | snv | 1 | |||
| rs4148388 | 1.000 | 0.160 | 10 | 99790008 | intron variant | G/A;C | snv | 1 | |||
| rs2756109 | 10 | 99798989 | intron variant | G/T | snv | 0.53 | 1 | ||||
| rs2002042 | 1.000 | 0.080 | 10 | 99828174 | intron variant | C/T | snv | 0.27 | 1 |