| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs10863246 | 1 | 216514743 | intron variant | G/A;C | snv | 0.28 | 1 | ||||
| rs10889584 | 1 | 65807607 | intron variant | C/T | snv | 0.18 | 1 | ||||
| rs10910953 | 1 | 181543317 | intron variant | G/T | snv | 0.14 | 1 | ||||
| rs10911009 | 1 | 182052669 | downstream gene variant | C/T | snv | 0.24 | 1 | ||||
| rs10913420 | 1 | 177790510 | intron variant | C/G;T | snv | 1 | |||||
| rs10917846 | 1 | 163782298 | intergenic variant | C/T | snv | 0.60 | 1 | ||||
| rs11122142 | 1 | 6769888 | intron variant | A/G;T | snv | 1 | |||||
| rs11207177 | 1 | 58217139 | intron variant | T/G | snv | 0.47 | 1 | ||||
| rs11208742 | 1 | 65773804 | regulatory region variant | C/T | snv | 0.17 | 1 | ||||
| rs11208757 | 1 | 65804253 | intron variant | C/T | snv | 0.18 | 1 | ||||
| rs11208774 | 1 | 65944426 | intron variant | C/T | snv | 0.41 | 1 | ||||
| rs11210274 | 1 | 73517390 | intergenic variant | G/T | snv | 0.54 | 1 | ||||
| rs11264489 | 1 | 156511039 | non coding transcript exon variant | A/G | snv | 0.34 | 1 | ||||
| rs113364618 | 1 | 72461657 | intron variant | G/A;C;T | snv | 1 | |||||
| rs113544820 | 1 | 155849227 | intron variant | G/A;T | snv | 3.5E-02 | 1 | ||||
| rs114667465 | 1 | 72015174 | intron variant | A/G | snv | 3.3E-02 | 1 | ||||
| rs11590190 | 1 | 243856696 | intergenic variant | A/G | snv | 0.14 | 1 | ||||
| rs116674558 | 1 | 98078517 | downstream gene variant | G/A | snv | 2.2E-02 | 1 | ||||
| rs1171044 | 1 | 190416174 | intron variant | C/T | snv | 0.73 | 1 | ||||
| rs11807366 | 1 | 73450965 | intergenic variant | A/C;G | snv | 1 | |||||
| rs1187769 | 1 | 213340893 | intergenic variant | C/T | snv | 0.21 | 1 | ||||
| rs12024115 | 1 | 41068685 | intron variant | C/T | snv | 0.11 | 1 | ||||
| rs12027943 | 1 | 216520449 | intron variant | C/A;T | snv | 1 | |||||
| rs12029493 | 1 | 41370133 | intron variant | T/C | snv | 0.13 | 1 | ||||
| rs12030690 | 1 | 37792335 | upstream gene variant | G/C | snv | 0.20 | 1 |