| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs11638027 | 1.000 | 0.080 | 15 | 90302268 | intron variant | G/T | snv | 9.9E-02 | 1 | ||
| rs12009 | 1.000 | 0.080 | 9 | 125235024 | 3 prime UTR variant | G/A;T | snv | 0.54 | 1 | ||
| rs12233338 | 1.000 | 0.080 | 21 | 33228611 | upstream gene variant | T/C | snv | 0.21 | 1 | ||
| rs12375841 | 1.000 | 0.080 | 9 | 4850141 | intron variant | T/C | snv | 0.33 | 1 | ||
| rs12484550 | 1.000 | 0.080 | 22 | 21587626 | intron variant | C/T | snv | 0.18 | 1 | ||
| rs12649554 | 1.000 | 0.080 | 4 | 100975519 | regulatory region variant | T/C | snv | 0.65 | 1 | ||
| rs12979680 | 1.000 | 0.080 | 19 | 21691444 | intergenic variant | C/A;T | snv | 1 | |||
| rs13213149 | 1.000 | 0.080 | 6 | 33071909 | intron variant | T/C | snv | 0.28 | 1 | ||
| rs1431399 | 1.000 | 0.080 | 6 | 33073257 | intron variant | A/G;T | snv | 1 | |||
| rs1431400 | 1.000 | 0.080 | 6 | 33073399 | intron variant | C/T | snv | 0.29 | 1 | ||
| rs1431401 | 1.000 | 0.080 | 6 | 33073409 | intron variant | G/A | snv | 0.29 | 1 | ||
| rs1442820036 | 1.000 | 0.080 | 21 | 33246788 | missense variant | G/A | snv | 4.0E-06 | 1 | ||
| rs146352658 | 1.000 | 0.080 | 9 | 21384972 | missense variant | C/T | snv | 7.6E-04 | 2.4E-04 | 1 | |
| rs149505691 | 1.000 | 0.080 | 8 | 144505069 | missense variant | G/A | snv | 1.5E-04 | 6.3E-05 | 1 | |
| rs1519551 | 1.000 | 0.080 | 4 | 141649319 | intron variant | G/A | snv | 0.55 | 1 | ||
| rs154977 | 1.000 | 0.080 | 6 | 32932241 | downstream gene variant | C/G;T | snv | 1 | |||
| rs17056316 | 1.000 | 0.080 | 4 | 170892334 | downstream gene variant | A/G | snv | 2.6E-03 | 1 | ||
| rs17214519 | 1.000 | 0.080 | 6 | 33064411 | downstream gene variant | G/A;T | snv | 1 | |||
| rs17385627 | 1.000 | 0.080 | 13 | 76953629 | synonymous variant | T/A | snv | 0.13 | 0.11 | 1 | |
| rs17470171 | 1.000 | 0.080 | 13 | 76946724 | upstream gene variant | C/A | snv | 0.11 | 1 | ||
| rs17780725 | 1.000 | 0.080 | 10 | 48422844 | intron variant | G/A | snv | 0.17 | 1 | ||
| rs1897824 | 1.000 | 0.080 | 19 | 44472854 | non coding transcript exon variant | T/A;C | snv | 1 | |||
| rs2051598 | 1.000 | 0.080 | 6 | 32741586 | intron variant | G/A | snv | 0.71 | 1 | ||
| rs2071351 | 1.000 | 0.080 | 6 | 33076153 | intron variant | A/G | snv | 0.24 | 0.29 | 1 | |
| rs2071353 | 1.000 | 0.080 | 6 | 33076480 | intron variant | T/C;G | snv | 1 |