| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs2476601 | 0.498 | 0.800 | 1 | 113834946 | missense variant | A/G | snv | 0.93 | 0.93 | 13 | |
| rs3748816 | 0.827 | 0.200 | 1 | 2595307 | missense variant | A/G | snv | 0.41 | 0.46 | 6 | |
| rs10903122 | 0.882 | 0.200 | 1 | 24977085 | intergenic variant | A/G | snv | 0.56 | 5 | ||
| rs11209026 | 0.597 | 0.680 | 1 | 67240275 | missense variant | G/A | snv | 4.2E-02 | 4.6E-02 | 5 | |
| rs1801274 | 0.597 | 0.800 | 1 | 161509955 | missense variant | A/C;G | snv | 4.0E-06; 0.48 | 5 | ||
| rs2228145 | 0.602 | 0.720 | 1 | 154454494 | missense variant | A/C;T | snv | 0.38; 1.2E-05 | 5 | ||
| rs2816316 | 0.882 | 0.200 | 1 | 192567683 | intron variant | C/A | snv | 0.79 | 5 | ||
| rs296547 | 0.882 | 0.200 | 1 | 200923009 | intron variant | T/C | snv | 0.53 | 5 | ||
| rs4129267 | 0.807 | 0.200 | 1 | 154453788 | intron variant | C/G;T | snv | 5 | |||
| rs11584383 | 0.827 | 0.200 | 1 | 200966738 | downstream gene variant | T/C | snv | 0.24 | 4 | ||
| rs9286879 | 0.851 | 0.200 | 1 | 172893094 | intron variant | A/G | snv | 0.32 | 4 | ||
| rs11465804 | 0.752 | 0.320 | 1 | 67236843 | intron variant | T/G | snv | 4.4E-02 | 5.4E-02 | 3 | |
| rs2274910 | 0.827 | 0.200 | 1 | 160882256 | non coding transcript exon variant | T/C | snv | 0.65 | 0.58 | 3 | |
| rs2814778 | 0.763 | 0.360 | 1 | 159204893 | 5 prime UTR variant | T/C | snv | 0.25 | 3 | ||
| rs12734001 | 1.000 | 0.080 | 1 | 202421786 | intron variant | C/T | snv | 3.5E-05 | 2 | ||
| rs1317209 | 0.925 | 0.120 | 1 | 19813543 | upstream gene variant | G/A;T | snv | 0.24 | 2 | ||
| rs3093059 | 0.752 | 0.520 | 1 | 159715346 | upstream gene variant | A/G | snv | 0.13 | 2 | ||
| rs7523907 | 1.000 | 0.080 | 1 | 167458010 | non coding transcript exon variant | C/A;T | snv | 2 | |||
| rs10800812 | 1.000 | 0.080 | 1 | 202086810 | intergenic variant | A/G | snv | 0.77 | 1 | ||
| rs10924993 | 0.925 | 0.080 | 1 | 236296485 | intergenic variant | T/A;G | snv | 1 | |||
| rs1101999 | 1.000 | 0.080 | 1 | 158962765 | intron variant | C/T | snv | 0.92 | 1 | ||
| rs1205 | 0.602 | 0.680 | 1 | 159712443 | 3 prime UTR variant | C/T | snv | 0.30 | 1 | ||
| rs148728975 | 1.000 | 0.080 | 1 | 12359827 | intron variant | G/A | snv | 3.7E-03 | 1 | ||
| rs1538084 | 1.000 | 0.080 | 1 | 152523536 | intergenic variant | A/C | snv | 0.79 | 1 | ||
| rs1775456 | 1.000 | 0.080 | 1 | 197763925 | intron variant | G/A | snv | 0.85 | 1 |