| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs10484545 | 1.000 | 0.040 | 6 | 29266733 | intron variant | C/A;G | snv | 1 | |||
| rs10486483 | 1.000 | 0.040 | 7 | 26852821 | intron variant | G/A | snv | 0.21 | 1 | ||
| rs10489276 | 1.000 | 0.040 | 1 | 172893799 | intron variant | C/T | snv | 0.31 | 1 | ||
| rs10512734 | 1.000 | 0.040 | 5 | 40393503 | intergenic variant | A/C;G | snv | 0.29 | 1 | ||
| rs10734105 | 1.000 | 0.040 | 10 | 131373856 | intergenic variant | G/A;C;T | snv | 1 | |||
| rs10789230 | 1.000 | 0.040 | 1 | 67264945 | downstream gene variant | G/C;T | snv | 1 | |||
| rs10801047 | 1.000 | 0.040 | 1 | 191590226 | intergenic variant | A/T | snv | 0.82 | 1 | ||
| rs10886462 | 1.000 | 0.040 | 10 | 119345799 | intron variant | A/G | snv | 0.22 | 1 | ||
| rs11010067 | 0.925 | 0.040 | 10 | 35006503 | downstream gene variant | C/G | snv | 0.37 | 1 | ||
| rs1105267 | 1.000 | 0.040 | 13 | 20365097 | intergenic variant | G/A | snv | 0.54 | 1 | ||
| rs1109863 | 1.000 | 0.040 | 16 | 50658453 | intergenic variant | G/A | snv | 0.69 | 1 | ||
| rs11190141 | 1.000 | 0.040 | 10 | 99532633 | upstream gene variant | C/T | snv | 0.40 | 1 | ||
| rs11195128 | 1.000 | 0.040 | 10 | 110426390 | downstream gene variant | C/G;T | snv | 1 | |||
| rs11208994 | 1.000 | 0.040 | 1 | 67059360 | regulatory region variant | A/G;T | snv | 1 | |||
| rs11209002 | 1.000 | 0.040 | 1 | 67124778 | intron variant | T/C | snv | 0.77 | 1 | ||
| rs11209003 | 1.000 | 0.040 | 1 | 67135449 | intron variant | G/T | snv | 0.28 | 1 | ||
| rs11229030 | 1.000 | 0.040 | 11 | 57435536 | regulatory region variant | C/T | snv | 0.55 | 1 | ||
| rs11265519 | 1.000 | 0.040 | 1 | 160909123 | intergenic variant | C/A | snv | 0.60 | 1 | ||
| rs1142287 | 1.000 | 0.040 | 1 | 155260340 | synonymous variant | C/T | snv | 0.34 | 0.36 | 1 | |
| rs11465802 | 1.000 | 0.040 | 1 | 67219915 | intron variant | A/C;T | snv | 1 | |||
| rs11574514 | 1.000 | 0.040 | 16 | 67937477 | upstream gene variant | C/T | snv | 2.9E-02 | 1 | ||
| rs11640716 | 1.000 | 0.040 | 16 | 50631178 | intron variant | T/A;G | snv | 1 | |||
| rs11718165 | 1.000 | 0.040 | 3 | 49659364 | intron variant | A/G | snv | 0.27 | 1 | ||
| rs11741861 | 0.925 | 0.040 | 5 | 150898347 | intron variant | A/G | snv | 8.8E-02 | 1 | ||
| rs11804284 | 1.000 | 0.040 | 1 | 67233571 | intron variant | T/A;C;G | snv | 1 |