| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs7763822 | 1.000 | 0.040 | 6 | 33092651 | intron variant | C/T | snv | 5.4E-02 | 1 | ||
| rs7764491 | 1.000 | 0.040 | 6 | 33093063 | non coding transcript exon variant | C/G | snv | 5.4E-02 | 1 | ||
| rs10186029 | 1.000 | 0.040 | 2 | 213064562 | intron variant | C/T | snv | 0.40 | 1 | ||
| rs589446 | 1.000 | 0.040 | 3 | 160015740 | non coding transcript exon variant | G/T | snv | 0.29 | 1 | ||
| rs2305743 | 1.000 | 0.040 | 19 | 18082381 | intron variant | G/A | snv | 0.19 | 1 | ||
| rs2201584 | 1.000 | 0.040 | 1 | 67322032 | intron variant | G/A | snv | 0.14 | 1 | ||
| rs3790566 | 1.000 | 0.040 | 1 | 67348757 | intron variant | T/C | snv | 0.61 | 1 | ||
| rs2069827 | 1.000 | 0.040 | 7 | 22725837 | non coding transcript exon variant | G/C;T | snv | 1 | |||
| rs2359661 | 1.000 | 0.040 | 16 | 31269826 | intron variant | A/G | snv | 0.48 | 1 | ||
| rs7190018 | 1.000 | 0.040 | 16 | 31290157 | intron variant | G/A;C | snv | 1 | |||
| rs4941246 | 1.000 | 0.040 | 18 | 64135070 | intron variant | C/T | snv | 0.60 | 1 | ||
| rs10220668 | 1.000 | 0.040 | 14 | 59042487 | intron variant | A/G | snv | 0.30 | 1 | ||
| rs11117420 | 1.000 | 0.040 | 16 | 85938316 | intron variant | G/C;T | snv | 1 | |||
| rs12039904 | 1.000 | 0.040 | 1 | 173243134 | intergenic variant | C/T | snv | 0.19 | 1 | ||
| rs1857066 | 1.000 | 0.040 | 1 | 173363490 | non coding transcript exon variant | A/C | snv | 0.79 | 1 | ||
| rs3104398 | 1.000 | 0.040 | 6 | 32717908 | upstream gene variant | G/A | snv | 0.12 | 1 | ||
| rs4648133 | 1.000 | 0.040 | 4 | 102615256 | intron variant | T/C | snv | 0.26 | 1 | ||
| rs7900522 | 1.000 | 0.040 | 10 | 76350213 | intron variant | T/A;C | snv | 1 | |||
| rs34826052 | 1.000 | 0.040 | 19 | 35345697 | synonymous variant | C/A;T | snv | 4.0E-02; 7.6E-05 | 1 | ||
| rs11538960 | 1.000 | 0.040 | 1 | 112701565 | missense variant | C/T | snv | 4.2E-04 | 5.2E-04 | 1 | |
| rs3802954 | 1.000 | 0.040 | 11 | 60470665 | 3 prime UTR variant | T/C | snv | 6.0E-02 | 1 | ||
| rs4939364 | 1.000 | 0.040 | 11 | 60464852 | intron variant | A/G | snv | 0.66 | 1 | ||
| rs7126354 | 1.000 | 0.040 | 11 | 60463593 | intron variant | C/T | snv | 0.64 | 1 | ||
| rs564732150 | 1.000 | 0.040 | 6 | 31028355 | missense variant | C/T | snv | 1 | |||
| rs16832798 | 1.000 | 0.040 | 2 | 190669646 | intron variant | T/C | snv | 0.19 | 1 |