| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs779738653 | 1.000 | 0.080 | 8 | 11847083 | frameshift variant | GA/- | delins | 4.0E-05 | 2.8E-05 | 1 | |
| rs1029153 | 1.000 | 0.080 | 10 | 44371698 | 3 prime UTR variant | A/G | snv | 0.27 | 1 | ||
| rs944459 | 1.000 | 0.080 | 14 | 64232640 | 3 prime UTR variant | C/T | snv | 1.1E-02 | 1 | ||
| rs1178326401 | 1.000 | 0.080 | 11 | 46728826 | synonymous variant | G/A | snv | 4.0E-06 | 1 | ||
| rs1754257 | 1.000 | 0.080 | 10 | 25385685 | intron variant | G/A | snv | 0.71 | 1 | ||
| rs747620337 | 1.000 | 0.080 | 8 | 144504414 | missense variant | T/C | snv | 4.0E-06 | 2.8E-05 | 1 | |
| rs1303234079 | 1.000 | 0.080 | 7 | 143267656 | missense variant | G/A | snv | 8.0E-06 | 1.4E-05 | 1 | |
| rs879097453 | 1.000 | 0.080 | 7 | 143265168 | missense variant | G/A | snv | 4.1E-06 | 1 | ||
| rs1063478 | 1.000 | 0.080 | 6 | 32949767 | missense variant | C/T | snv | 0.15 | 0.13 | 1 | |
| rs2284191 | 1.000 | 0.080 | 6 | 33008877 | intron variant | G/A | snv | 7.5E-02 | 1 | ||
| rs3212172 | 1.000 | 0.080 | 20 | 44399750 | intron variant | A/C;G | snv | 1 | |||
| rs1156458285 | 1.000 | 0.080 | 9 | 21440717 | missense variant | G/C | snv | 1 | |||
| rs1236515917 | 1.000 | 0.080 | 9 | 21367798 | missense variant | C/G | snv | 4.4E-06 | 1 | ||
| rs74597329 | 1.000 | 0.080 | 19 | 39248515 | missense variant | T/A;G | snv | 0.22 | 1 | ||
| rs11249006 | 1.000 | 0.080 | 1 | 24155984 | 3 prime UTR variant | G/A | snv | 0.30 | 1 | ||
| rs4489498 | 1.000 | 0.080 | 1 | 24185565 | intron variant | C/T | snv | 0.88 | 1 | ||
| rs7532146 | 1.000 | 0.080 | 1 | 24184442 | intron variant | T/C | snv | 9.2E-02 | 1 | ||
| rs749041212 | 1.000 | 0.080 | 16 | 27363054 | missense variant | G/A | snv | 4.0E-06 | 7.0E-06 | 1 | |
| rs987106 | 1.000 | 0.080 | 5 | 35875491 | non coding transcript exon variant | A/T | snv | 0.49 | 0.53 | 1 | |
| rs373743090 | 1.000 | 0.080 | X | 154016502 | missense variant | G/A;C | snv | 5.5E-06 | 1 | ||
| rs779916209 | 1.000 | 0.080 | 2 | 8802958 | missense variant | G/C | snv | 4.0E-06 | 1 | ||
| rs2569540 | 1.000 | 0.080 | 19 | 11127563 | non coding transcript exon variant | C/G | snv | 0.68 | 1 | ||
| rs4075184 | 1.000 | 0.080 | 1 | 25564344 | non coding transcript exon variant | G/A | snv | 0.52 | 1 | ||
| rs1049807 | 1.000 | 0.080 | 17 | 36105270 | missense variant | A/G | snv | 0.22 | 0.21 | 1 | |
| rs201065145 | 1.000 | 0.080 | 8 | 144505096 | missense variant | G/A | snv | 1.4E-04 | 3.5E-05 | 1 |