| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs1029153 | 1.000 | 0.080 | 10 | 44371698 | 3 prime UTR variant | A/G | snv | 0.27 | 1 | ||
| rs1034713634 | 1.000 | 0.080 | 3 | 42536097 | missense variant | C/A;T | snv | 1 | |||
| rs1049807 | 1.000 | 0.080 | 17 | 36105270 | missense variant | A/G | snv | 0.22 | 0.21 | 1 | |
| rs1052020291 | 1.000 | 0.080 | 8 | 11848075 | missense variant | G/C | snv | 7.0E-06 | 1 | ||
| rs1063340 | 1.000 | 0.080 | 17 | 36088417 | 3 prime UTR variant | G/C;T | snv | 1 | |||
| rs1063478 | 1.000 | 0.080 | 6 | 32949767 | missense variant | C/T | snv | 0.15 | 0.13 | 1 | |
| rs111511318 | 1.000 | 0.080 | 5 | 156998817 | intergenic variant | C/A | snv | 2.9E-02 | 1 | ||
| rs11249006 | 1.000 | 0.080 | 1 | 24155984 | 3 prime UTR variant | G/A | snv | 0.30 | 1 | ||
| rs1156458285 | 1.000 | 0.080 | 9 | 21440717 | missense variant | G/C | snv | 1 | |||
| rs116399066 | 1.000 | 0.080 | 1 | 143723149 | upstream gene variant | C/A;T | snv | 1 | |||
| rs1178326401 | 1.000 | 0.080 | 11 | 46728826 | synonymous variant | G/A | snv | 4.0E-06 | 1 | ||
| rs1236515917 | 1.000 | 0.080 | 9 | 21367798 | missense variant | C/G | snv | 4.4E-06 | 1 | ||
| rs1303234079 | 1.000 | 0.080 | 7 | 143267656 | missense variant | G/A | snv | 8.0E-06 | 1.4E-05 | 1 | |
| rs13401937 | 1.000 | 0.080 | 2 | 55025078 | splice region variant | T/G | snv | 0.11 | 0.14 | 1 | |
| rs1484994 | 1.000 | 0.080 | 20 | 31718172 | intron variant | A/G | snv | 0.38 | 1 | ||
| rs1754257 | 1.000 | 0.080 | 10 | 25385685 | intron variant | G/A | snv | 0.71 | 1 | ||
| rs179012 | 1.000 | 0.080 | X | 12883443 | intron variant | G/A | snv | 0.42 | 1 | ||
| rs179016 | 1.000 | 0.080 | X | 12876323 | intron variant | G/A;C;T | snv | 1 | |||
| rs1800803 | 1.000 | 0.080 | 4 | 99574424 | intron variant | A/T | snv | 0.43 | 1 | ||
| rs1979860 | 1.000 | 0.080 | 5 | 174586529 | regulatory region variant | C/T | snv | 1.8E-02 | 1 | ||
| rs1997060 | 1.000 | 0.080 | 3 | 174035108 | intron variant | A/G | snv | 0.18 | 1 | ||
| rs200664537 | 1.000 | 0.080 | 8 | 11847084 | missense variant | G/A;C | snv | 4.0E-06; 1.2E-04 | 1 | ||
| rs201065145 | 1.000 | 0.080 | 8 | 144505096 | missense variant | G/A | snv | 1.4E-04 | 3.5E-05 | 1 | |
| rs2233437 | 1.000 | 0.080 | 6 | 44260425 | intron variant | G/A | snv | 0.43 | 0.35 | 1 | |
| rs2278034 | 1.000 | 0.080 | 3 | 195870036 | 3 prime UTR variant | T/C;G | snv | 0.44; 2.7E-05 | 1 |