| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs11190140 | 0.827 | 0.160 | 10 | 99531836 | upstream gene variant | T/C | snv | 0.55 | 6 | ||
| rs1384936174 | 0.827 | 0.040 | 16 | 50710812 | missense variant | G/A;T | snv | 4.0E-06; 4.0E-06 | 6 | ||
| rs2349775 | 0.851 | 0.120 | 7 | 8678450 | intron variant | G/A;C | snv | 6 | |||
| rs3129891 | 0.851 | 0.160 | 6 | 32447303 | downstream gene variant | G/A | snv | 0.20 | 5 | ||
| rs1800870 | 0.851 | 0.200 | 17 | 19649164 | intron variant | C/T | snv | 5 | |||
| rs4722999 | 0.851 | 0.080 | 7 | 30654159 | intron variant | C/T | snv | 0.67 | 5 | ||
| rs7209436 | 0.851 | 0.200 | 17 | 45792776 | intron variant | C/T | snv | 0.43 | 5 | ||
| rs199473072 | 0.827 | 0.160 | 3 | 38613773 | missense variant | G/A | snv | 1.2E-05 | 8.4E-05 | 5 | |
| rs3765534 | 0.882 | 0.200 | 13 | 95163161 | missense variant | C/T | snv | 2.3E-02 | 1.2E-02 | 4 | |
| rs4537731 | 1.000 | 0.040 | 11 | 18047335 | upstream gene variant | T/C | snv | 0.48 | 3 | ||
| rs11554825 | 0.882 | 0.120 | 2 | 218261086 | 5 prime UTR variant | C/T | snv | 0.44 | 3 | ||
| rs242924 | 0.882 | 0.080 | 17 | 45808001 | intron variant | G/T | snv | 0.44 | 3 | ||
| rs62636489 | 0.925 | 0.040 | 12 | 52898860 | missense variant | G/A | snv | 7.6E-05 | 7.0E-06 | 3 | |
| rs77005575 | 1.000 | 0.040 | 6 | 32611931 | intergenic variant | T/C | snv | 2 | |||
| rs149382949 | 1.000 | 0.040 | 2 | 219232579 | missense variant | G/A;C | snv | 3.2E-05; 4.0E-06 | 2 | ||
| rs806378 | 1.000 | 0.040 | 6 | 88149832 | intron variant | C/T | snv | 0.21 | 2 | ||
| rs10474485 | 1.000 | 0.040 | 5 | 76975028 | intron variant | C/A | snv | 0.26 | 2 | ||
| rs3779250 | 0.925 | 0.080 | 7 | 30654644 | intron variant | C/T | snv | 0.48 | 2 | ||
| rs201253747 | 1.000 | 0.040 | 5 | 148483142 | 3 prime UTR variant | A/G | snv | 2.1E-03 | 2 | ||
| rs137854608 | 0.925 | 0.120 | 3 | 38609776 | missense variant | C/T | snv | 2.4E-05 | 3.5E-05 | 2 | |
| rs41311127 | 0.925 | 0.120 | 3 | 38562500 | missense variant | A/G | snv | 6.5E-04 | 4.7E-04 | 2 | |
| rs750438327 | 1.000 | 0.040 | 8 | 132888076 | missense variant | G/A;C | snv | 7.6E-05 | 2 | ||
| rs7130929 | 1.000 | 0.040 | 11 | 18046616 | upstream gene variant | C/A | snv | 0.40 | 1 | ||
| 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 |