| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs200378616 | 0.882 | 0.120 | 7 | 87544938 | missense variant | G/C;T | snv | 4.0E-05; 8.0E-06 | 3 | ||
| rs1169704167 | 0.882 | 0.120 | 11 | 108284370 | frameshift variant | -/T | delins | 8.0E-06 | 3 | ||
| rs35134728 | 0.882 | 0.120 | 1 | 11787277 | 3 prime UTR variant | -/AGA | delins | 3 | |||
| rs3737966 | 0.882 | 0.120 | 1 | 11787702 | 3 prime UTR variant | C/T | snv | 0.55 | 3 | ||
| rs3731246 | 0.882 | 0.120 | 9 | 21971990 | intron variant | C/G | snv | 0.11 | 3 | ||
| rs12434881 | 0.882 | 0.120 | 14 | 23119433 | 5 prime UTR variant | G/A | snv | 0.36 | 3 | ||
| rs1296957097 | 0.882 | 0.120 | 22 | 28719401 | missense variant | A/G | snv | 3 | |||
| rs759602460 | 0.882 | 0.120 | 18 | 74518552 | missense variant | C/G | snv | 1.6E-05; 4.0E-06 | 3 | ||
| rs140422742 | 0.882 | 0.120 | 7 | 99778046 | missense variant | T/C;G | snv | 7.6E-05 | 6.3E-05 | 3 | |
| rs368005287 | 0.882 | 0.120 | 7 | 99762071 | stop gained | C/T | snv | 1.2E-05 | 7.0E-06 | 3 | |
| rs777926364 | 0.882 | 0.120 | 7 | 99664017 | missense variant | C/T | snv | 4.2E-06 | 3 | ||
| rs7809758 | 0.882 | 0.120 | 7 | 50505635 | intron variant | A/G | snv | 0.36 | 3 | ||
| rs7286979 | 0.882 | 0.120 | 22 | 41102623 | intron variant | G/A | snv | 0.26 | 3 | ||
| rs1573613 | 0.882 | 0.120 | 12 | 11894684 | 3 prime UTR variant | T/C | snv | 0.48 | 3 | ||
| rs880028 | 0.882 | 0.120 | 7 | 50502438 | intron variant | A/G | snv | 0.21 | 3 | ||
| rs7039798 | 0.882 | 0.120 | 9 | 127794947 | intron variant | G/A;C | snv | 3 | |||
| rs3758149 | 0.882 | 0.120 | 8 | 63039169 | upstream gene variant | G/A | snv | 0.24 | 3 | ||
| rs104893636 | 0.882 | 0.120 | 2 | 176151875 | missense variant | A/C;T | snv | 5.2E-06; 7.9E-04 | 3 | ||
| rs10235796 | 0.882 | 0.120 | 7 | 50394939 | intron variant | T/C | snv | 0.82 | 3 | ||
| rs10519612 | 0.882 | 0.120 | 4 | 141732548 | intron variant | A/C | snv | 0.10 | 3 | ||
| rs41320251 | 0.882 | 0.120 | 20 | 3213196 | missense variant | C/A;G | snv | 3 | |||
| rs766916111 | 0.882 | 0.120 | 20 | 3223452 | missense variant | T/C | snv | 4.0E-06 | 7.0E-06 | 3 | |
| rs111978267 | 0.882 | 0.120 | 11 | 2751648 | intron variant | C/G;T | snv | 2.8E-05 | 3 | ||
| rs525549 | 0.882 | 0.120 | 11 | 118487353 | intron variant | T/A | snv | 0.33 | 3 | ||
| rs76996680 | 0.882 | 0.120 | 4 | 108163665 | missense variant | G/A | snv | 1.0E-03 | 3.4E-04 | 3 |