| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs1800470 | 0.515 | 0.840 | 19 | 41353016 | missense variant | G/A;C | snv | 0.55; 2.4E-04 | 107 | ||
| rs1800796 | 0.555 | 0.760 | 7 | 22726627 | non coding transcript exon variant | G/C | snv | 9.9E-02 | 74 | ||
| rs143383 | 0.724 | 0.320 | 20 | 35438203 | 5 prime UTR variant | G/A | snv | 0.47 | 17 | ||
| rs143384 | 0.827 | 0.200 | 20 | 35437976 | 5 prime UTR variant | G/A | snv | 0.44 | 17 | ||
| rs1554944271 | 0.851 | 0.240 | 11 | 686925 | missense variant | C/G | snv | 14 | |||
| rs1553525325 | 0.807 | 0.120 | 2 | 166002716 | missense variant | A/T | snv | 9 | |||
| rs1569198 | 0.851 | 0.200 | 10 | 52316511 | intron variant | A/G | snv | 0.41 | 0.42 | 4 | |
| rs6060373 | 0.925 | 0.200 | 20 | 35326405 | intron variant | A/G | snv | 0.49 | 4 | ||
| rs11718863 | 0.882 | 0.080 | 3 | 15175196 | non coding transcript exon variant | A/G;T | snv | 0.21 | 3 | ||
| rs7639618 | 0.882 | 0.080 | 3 | 15174922 | non coding transcript exon variant | C/T | snv | 0.22 | 0.18 | 3 | |
| rs763098832 | 0.882 | 0.120 | 19 | 18783189 | missense variant | G/C;T | snv | 4.1E-06 | 3 | ||
| rs867986409 | 0.882 | 0.120 | 19 | 18784246 | missense variant | C/T | snv | 8.0E-06 | 3 | ||
| rs61746008 | 0.882 | 0.160 | 15 | 48412619 | missense variant | G/A;C | snv | 7.3E-04 | 3 | ||
| rs764256352 | 0.882 | 0.120 | 5 | 149981625 | missense variant | G/C | snv | 4.0E-06 | 2.1E-05 | 3 | |
| rs9864422 | 0.925 | 0.080 | 3 | 15185745 | intron variant | C/T | snv | 0.17 | 2 | ||
| rs61930502 | 1.000 | 0.080 | 12 | 113547623 | regulatory region variant | A/G | snv | 0.28 | 1 | ||
| rs1022313 | 1.000 | 0.080 | 6 | 112053741 | upstream gene variant | G/A | snv | 0.22 | 1 | ||
| rs1230345 | 1.000 | 0.080 | 6 | 112061110 | missense variant | G/A;C;T | snv | 0.26 | 0.32 | 1 | |
| rs17073268 | 1.000 | 0.080 | 6 | 112062577 | intron variant | G/A | snv | 0.24 | 1 | ||
| rs2303486 | 1.000 | 0.080 | 17 | 48622307 | 3 prime UTR variant | A/T | snv | 0.47 | 1 | ||
| rs8844 | 1.000 | 0.080 | 17 | 48621348 | 3 prime UTR variant | C/G;T | snv | 1 | |||
| rs711819 | 1.000 | 0.080 | 2 | 176120968 | upstream gene variant | T/C | snv | 0.82 | 1 | ||
| rs726252 | 1.000 | 0.080 | 1 | 176691111 | 3 prime UTR variant | C/T | snv | 0.55 | 1 | ||
| rs3744438 | 1.000 | 0.080 | 17 | 61480239 | missense variant | C/A;T | snv | 4.0E-06; 0.14 | 1 | ||
| rs3744448 | 1.000 | 0.080 | 17 | 61456507 | missense variant | G/C;T | snv | 0.17; 1.1E-05 | 1 |