| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs9978223 | 1.000 | 0.080 | 21 | 33398052 | upstream gene variant | G/A | snv | 0.24 | 1 | ||
| rs760761240 | 1.000 | 0.080 | 17 | 34256290 | missense variant | G/A;C | snv | 6.0E-05 | 1 | ||
| rs754889760 | 1.000 | 0.080 | 22 | 50571440 | missense variant | T/C | snv | 4.0E-06 | 1 | ||
| rs1183027238 | 1.000 | 0.080 | 13 | 113118480 | synonymous variant | C/T | snv | 1 | |||
| rs200478651 | 1.000 | 0.080 | 13 | 113118414 | splice region variant | C/A;T | snv | 8.4E-06; 2.1E-05 | 1 | ||
| rs1445501474 | 1.000 | 0.080 | 18 | 22168521 | intron variant | G/T | snv | 1.4E-05 | 1 | ||
| rs1416421760 | 1.000 | 0.080 | 18 | 22168362 | non coding transcript exon variant | C/A | snv | 1.4E-05 | 1 | ||
| rs1201493098 | 1.000 | 0.080 | 17 | 4934295 | missense variant | A/G | snv | 4.0E-06 | 1.4E-05 | 1 | |
| rs1175571390 | 1.000 | 0.080 | 5 | 53056071 | missense variant | T/C | snv | 1 | |||
| rs2804924 | 1.000 | 0.080 | 6 | 13574110 | upstream gene variant | G/A;C;T | snv | 1 | |||
| rs1140713 | 1.000 | 0.080 | 9 | 136670833 | intron variant | C/T | snv | 0.13 | 1 | ||
| rs775913429 | 1.000 | 0.080 | 12 | 132620455 | missense variant | G/A | snv | 8.0E-06 | 1.4E-05 | 1 | |
| rs766816990 | 1.000 | 0.080 | 17 | 3691667 | missense variant | C/A;T | snv | 4.0E-06; 1.2E-05 | 1 | ||
| rs1217035505 | 1.000 | 0.080 | 12 | 121184674 | missense variant | G/A | snv | 1 | |||
| rs12375498 | 1.000 | 0.080 | 9 | 116187719 | synonymous variant | C/T | snv | 0.19 | 0.17 | 1 | |
| rs112443954 | 1.000 | 0.080 | 6 | 13574259 | upstream gene variant | G/C | snv | 0.27 | 1 | ||
| rs12095080 | 1.000 | 0.080 | 1 | 53911057 | 3 prime UTR variant | A/G | snv | 0.12 | 2 | ||
| rs1226052130 | 0.925 | 0.120 | 17 | 47299308 | missense variant | G/A | snv | 4.0E-06 | 2 | ||
| rs740952 | 0.925 | 0.080 | 7 | 150952515 | synonymous variant | G/A;T | snv | 0.30; 7.2E-05 | 2 | ||
| rs201698592 | 0.925 | 0.080 | 11 | 2847916 | synonymous variant | C/T | snv | 1.7E-04 | 2.8E-05 | 2 | |
| rs12090554 | 0.925 | 0.080 | 1 | 185583216 | intron variant | G/A | snv | 0.15 | 2 | ||
| rs1076991 | 0.925 | 0.200 | 14 | 64388323 | 5 prime UTR variant | T/C;G | snv | 0.45; 8.1E-06 | 2 | ||
| rs3736235 | 0.925 | 0.080 | 12 | 10160476 | non coding transcript exon variant | T/C | snv | 0.43 | 0.40 | 2 | |
| rs13290387 | 0.925 | 0.120 | 9 | 116227647 | intron variant | G/C | snv | 0.54 | 2 | ||
| rs1353342 | 0.925 | 0.080 | 9 | 76259853 | intron variant | A/C | snv | 0.79 | 2 |