| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs1385526 | 1.000 | 0.040 | 12 | 57138966 | intron variant | G/C | snv | 0.26 | 1 | ||
| rs1419338705 | 1.000 | 0.040 | 7 | 74048163 | missense variant | C/T | snv | 7.0E-06 | 1 | ||
| rs1795061 | 1.000 | 0.040 | 1 | 214235937 | intergenic variant | T/C;G | snv | 1 | |||
| rs2652106 | 1.000 | 0.040 | 5 | 83498217 | intron variant | G/T | snv | 0.39 | 1 | ||
| rs2836411 | 1.000 | 0.040 | 21 | 38447907 | intron variant | C/A;T | snv | 1 | |||
| rs3781590 | 1.000 | 0.040 | 11 | 68391684 | intron variant | G/A | snv | 0.35 | 1 | ||
| rs58749629 | 1.000 | 0.040 | 20 | 45942678 | intron variant | G/A;T | snv | 0.13 | 1 | ||
| rs6674171 | 1.000 | 0.040 | 1 | 154519207 | intron variant | A/G;T | snv | 0.19 | 1 | ||
| rs9316871 | 1.000 | 0.040 | 13 | 22287782 | intergenic variant | A/G | snv | 0.22 | 1 | ||
| rs1217691063 | 0.330 | 0.920 | 1 | 11796309 | missense variant | A/G | snv | 4.0E-06 | 7.0E-06 | 614 | |
| rs763059810 | 0.623 | 0.600 | 2 | 136115750 | missense variant | T/C | snv | 4.0E-06 | 41 | ||
| rs1418184396 | 1.000 | 0.040 | 17 | 1776722 | missense variant | C/T | snv | 4.0E-06 | 1 | ||
| rs77294580 | 1.000 | 0.040 | 17 | 63480396 | missense variant | G/A;T | snv | 4.0E-06; 4.0E-06 | 1 | ||
| rs763351020 | 0.633 | 0.560 | 7 | 101132046 | missense variant | C/T | snv | 4.0E-06 | 35 | ||
| rs1265538677 | 0.790 | 0.200 | 13 | 46055808 | synonymous variant | A/G | snv | 4.0E-06 | 10 | ||
| rs201191171 | 0.925 | 0.080 | 20 | 46013279 | missense variant | G/A;C;T | snv | 4.0E-06; 4.0E-06 | 2 | ||
| rs3877899 | 0.827 | 0.160 | 5 | 42801166 | missense variant | C/A;T | snv | 4.0E-06; 0.20 | 7 | ||
| rs766407419 | 1.000 | 0.040 | 17 | 1745008 | missense variant | T/C | snv | 8.0E-06 | 1.4E-05 | 1 | |
| rs782591769 | 1.000 | 0.040 | 7 | 74045237 | missense variant | G/C | snv | 8.0E-06 | 1 | ||
| rs773474756 | 0.925 | 0.080 | 11 | 102790467 | missense variant | T/C | snv | 8.1E-06 | 2 | ||
| rs767169659 | 1.000 | 0.040 | 3 | 123733800 | missense variant | G/A | snv | 1.2E-05 | 1 | ||
| rs486055 | 0.925 | 0.120 | 11 | 102779693 | missense variant | C/G;T | snv | 1.2E-05; 0.10 | 3 | ||
| rs2228145 | 0.602 | 0.720 | 1 | 154454494 | missense variant | A/C;T | snv | 0.38; 1.2E-05 | 57 | ||
| rs2306691 | 1.000 | 0.040 | 12 | 57145019 | missense variant | A/G | snv | 2.0E-05 | 2.1E-05 | 1 | |
| rs121917864 | 0.645 | 0.520 | 4 | 153704936 | missense variant | C/T | snv | 8.8E-05 | 9.8E-05 | 31 |