| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs11085835 | 1.000 | 0.040 | 19 | 13221196 | intron variant | T/A;C | snv | 1 | |||
| rs116250606 | 1.000 | 0.040 | 10 | 103473496 | missense variant | C/T | snv | 6.5E-06; 4.1E-03 | 2.3E-02 | 1 | |
| rs116175374 | 1.000 | 0.040 | 2 | 31202319 | intron variant | G/A | snv | 4.9E-02 | 1 | ||
| rs17387019 | 1.000 | 0.040 | 12 | 25111325 | intron variant | G/A | snv | 5.7E-02 | 1 | ||
| rs1971256 | 1.000 | 0.040 | 6 | 151494876 | intron variant | T/C | snv | 0.37 | 1 | ||
| rs1447669065 | 1.000 | 0.040 | 11 | 35176638 | missense variant | T/C | snv | 4.0E-06 | 1 | ||
| rs756384853 | 1.000 | 0.040 | 11 | 35229167 | missense variant | A/C;G | snv | 4.0E-06; 4.0E-06 | 1 | ||
| rs200922190 | 1.000 | 0.040 | 1 | 193234361 | intron variant | -/ATAATT | delins | 0.16 | 1 | ||
| rs10965235 | 1.000 | 0.040 | 9 | 22115106 | intron variant | C/A | snv | 0.15 | 1 | ||
| rs9434741 | 1.000 | 0.040 | 1 | 6157799 | intron variant | A/G | snv | 0.26 | 1 | ||
| rs893363 | 1.000 | 0.040 | 3 | 53813035 | 3 prime UTR variant | G/A | snv | 0.54 | 1 | ||
| rs2289205 | 1.000 | 0.040 | 3 | 53844589 | 5 prime UTR variant | C/T | snv | 0.27 | 1 | ||
| rs7928739 | 1.000 | 0.040 | 11 | 68066076 | intron variant | C/A | snv | 0.52 | 1 | ||
| rs2300795 | 1.000 | 0.040 | 6 | 75115465 | intron variant | A/G | snv | 0.11 | 1 | ||
| rs7356530 | 1.000 | 0.040 | 5 | 79105085 | intron variant | G/A | snv | 0.52 | 1 | ||
| rs758316 | 1.000 | 0.040 | 7 | 153934563 | intron variant | G/A | snv | 0.64 | 1 | ||
| rs11977660 | 1.000 | 0.040 | 7 | 55094643 | intron variant | T/C | snv | 0.42 | 1 | ||
| rs1159327 | 1.000 | 0.040 | 6 | 151726887 | intron variant | C/T | snv | 0.32 | 1 | ||
| rs2206949 | 1.000 | 0.040 | 6 | 151716421 | intron variant | C/T | snv | 0.32 | 1 | ||
| rs3798573 | 1.000 | 0.040 | 6 | 152068227 | intron variant | A/G | snv | 0.22 | 1 | ||
| rs9340773 | 1.000 | 0.040 | 6 | 151808141 | missense variant | G/A;C | snv | 4.6E-03; 4.5E-06 | 1 | ||
| rs17179740 | 1.000 | 0.040 | 14 | 64290033 | intron variant | G/A | snv | 0.44 | 1 | ||
| rs751676149 | 1.000 | 0.040 | 14 | 64233228 | missense variant | C/T | snv | 2.8E-05 | 2.1E-05 | 1 | |
| rs10777670 | 1.000 | 0.040 | 12 | 95181055 | intron variant | G/A | snv | 0.23 | 1 | ||
| rs62469231 | 1.000 | 0.040 | 7 | 114391119 | intron variant | G/A | snv | 1.1E-02 | 1 |