| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs10503256 | 1.000 | 0.040 | 8 | 4356657 | intron variant | A/G | snv | 0.57 | 1 | ||
| rs10503899 | 1.000 | 0.040 | 8 | 32089718 | intron variant | A/G | snv | 0.33 | 1 | ||
| rs1064627 | 1.000 | 0.040 | 6 | 30730764 | non coding transcript exon variant | A/G | snv | 0.17 | 0.19 | 1 | |
| rs10750489 | 1.000 | 0.040 | 11 | 131786445 | intron variant | C/G;T | snv | 0.91 | 1 | ||
| rs10789369 | 1.000 | 0.040 | 1 | 73359226 | downstream gene variant | A/G;T | snv | 1 | |||
| rs10791946 | 1.000 | 0.040 | 11 | 67820541 | intron variant | A/G | snv | 0.41 | 1 | ||
| rs10812518 | 1.000 | 0.040 | 9 | 27041678 | intron variant | C/T | snv | 0.30 | 1 | ||
| rs10894294 | 1.000 | 0.040 | 11 | 130960853 | intergenic variant | C/A;G | snv | 1 | |||
| rs10970384 | 1.000 | 0.040 | 9 | 3158247 | intergenic variant | A/C | snv | 0.21 | 1 | ||
| rs10973441 | 1.000 | 0.040 | 9 | 37622780 | intron variant | T/C | snv | 0.14 | 1 | ||
| rs10976131 | 1.000 | 0.040 | 9 | 7226519 | intergenic variant | T/C | snv | 0.18 | 1 | ||
| rs11038167 | 1.000 | 0.040 | 11 | 44821583 | intron variant | A/C;G | snv | 1 | |||
| rs11038172 | 1.000 | 0.040 | 11 | 44834046 | intron variant | A/G | snv | 5.1E-02 | 1 | ||
| rs11055980 | 1.000 | 0.040 | 12 | 14458588 | intron variant | C/T | snv | 0.40 | 1 | ||
| rs11060225 | 1.000 | 0.040 | 12 | 129254501 | intron variant | A/G | snv | 6.9E-02 | 1 | ||
| rs11064768 | 1.000 | 0.040 | 12 | 119380704 | intron variant | A/G | snv | 5.6E-02 | 1 | ||
| rs11165389 | 1.000 | 0.040 | 1 | 95350307 | downstream gene variant | T/G | snv | 0.33 | 1 | ||
| rs11191732 | 1.000 | 0.040 | 10 | 103572004 | intron variant | G/A | snv | 0.14 | 1 | ||
| rs11220082 | 1.000 | 0.040 | 11 | 125454069 | intron variant | C/T | snv | 0.46 | 1 | ||
| rs11242417 | 1.000 | 0.040 | 5 | 138263645 | intron variant | T/G | snv | 0.13 | 1 | ||
| rs11532322 | 1.000 | 0.040 | 12 | 123246876 | intron variant | A/G;T | snv | 1 | |||
| rs11562926 | 1.000 | 0.040 | 4 | 117728887 | intergenic variant | T/C | snv | 0.29 | 1 | ||
| rs11747553 | 1.000 | 0.040 | 5 | 55473592 | intron variant | G/A | snv | 0.67 | 1 | ||
| rs11819869 | 1.000 | 0.040 | 11 | 46539130 | intron variant | C/T | snv | 0.27 | 1 | ||
| rs11945758 | 1.000 | 0.040 | 4 | 117746079 | intergenic variant | G/A;T | snv | 1 |