| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs3779250 | 0.925 | 0.080 | 7 | 30654644 | intron variant | C/T | snv | 0.48 | 2 | ||
| rs77005575 | 1.000 | 0.040 | 6 | 32611931 | intergenic variant | T/C | snv | 2 | |||
| rs806378 | 1.000 | 0.040 | 6 | 88149832 | intron variant | C/T | snv | 0.21 | 2 | ||
| rs17837965 | 1.000 | 0.040 | 1 | 22068132 | intron variant | A/G | snv | 5.3E-02 | 1 | ||
| rs245051 | 1.000 | 0.040 | 5 | 149966412 | intron variant | A/G;T | snv | 1 | |||
| rs684302 | 1.000 | 0.040 | 11 | 18038806 | intron variant | C/T | snv | 0.36 | 1 | ||
| rs7130929 | 1.000 | 0.040 | 11 | 18046616 | upstream gene variant | C/A | snv | 0.40 | 1 | ||
| rs9999118 | 1.000 | 0.040 | 4 | 123130312 | intron variant | A/G | snv | 1.2E-02 | 1 | ||
| rs1384936174 | 0.827 | 0.040 | 16 | 50710812 | missense variant | G/A;T | snv | 4.0E-06; 4.0E-06 | 6 | ||
| rs149382949 | 1.000 | 0.040 | 2 | 219232579 | missense variant | G/A;C | snv | 3.2E-05; 4.0E-06 | 2 | ||
| rs199473072 | 0.827 | 0.160 | 3 | 38613773 | missense variant | G/A | snv | 1.2E-05 | 8.4E-05 | 5 | |
| rs137854608 | 0.925 | 0.120 | 3 | 38609776 | missense variant | C/T | snv | 2.4E-05 | 3.5E-05 | 2 | |
| rs750438327 | 1.000 | 0.040 | 8 | 132888076 | missense variant | G/A;C | snv | 7.6E-05 | 2 | ||
| rs62636489 | 0.925 | 0.040 | 12 | 52898860 | missense variant | G/A | snv | 7.6E-05 | 7.0E-06 | 3 | |
| rs41311127 | 0.925 | 0.120 | 3 | 38562500 | missense variant | A/G | snv | 6.5E-04 | 4.7E-04 | 2 | |
| rs3765534 | 0.882 | 0.200 | 13 | 95163161 | missense variant | C/T | snv | 2.3E-02 | 1.2E-02 | 4 | |
| rs116855232 | 0.742 | 0.400 | 13 | 48045719 | missense variant | C/T | snv | 2.8E-02 | 1.1E-02 | 12 | |
| rs11465804 | 0.752 | 0.320 | 1 | 67236843 | intron variant | T/G | snv | 4.4E-02 | 5.4E-02 | 10 | |
| rs1800629 | 0.472 | 0.920 | 6 | 31575254 | upstream gene variant | G/A | snv | 0.12 | 0.14 | 169 | |
| rs1801725 | 0.633 | 0.600 | 3 | 122284910 | missense variant | G/T | snv | 0.13 | 0.11 | 39 | |
| rs324420 | 0.637 | 0.440 | 1 | 46405089 | missense variant | C/A | snv | 0.24 | 0.26 | 48 | |
| rs224222 | 0.724 | 0.440 | 16 | 3254463 | missense variant | C/T | snv | 0.24 | 0.21 | 15 | |
| rs5443 | 0.532 | 0.760 | 12 | 6845711 | synonymous variant | C/T | snv | 0.36 | 0.44 | 106 | |
| rs6313 | 0.562 | 0.640 | 13 | 46895805 | synonymous variant | G/A | snv | 0.41 | 0.40 | 82 | |
| rs2241880 | 0.627 | 0.600 | 2 | 233274722 | missense variant | A/G | snv | 0.45 | 0.44 | 37 |