| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs10757279 | 0.925 | 0.040 | 9 | 22124631 | intron variant | A/G | snv | 0.40 | 3 | ||
| rs10811647 | 1.000 | 0.040 | 9 | 22065003 | intron variant | C/G;T | snv | 3 | |||
| rs10965212 | 0.925 | 0.080 | 9 | 22023796 | intron variant | T/A;C;G | snv | 3 | |||
| rs1333037 | 0.925 | 0.040 | 9 | 22040766 | intron variant | C/T | snv | 0.71 | 3 | ||
| rs1537373 | 0.925 | 0.120 | 9 | 22103342 | intron variant | T/G | snv | 0.63 | 3 | ||
| rs1537374 | 1.000 | 0.040 | 9 | 22116047 | intron variant | A/G | snv | 0.64 | 3 | ||
| rs2069416 | 0.925 | 0.040 | 9 | 22010005 | intron variant | T/A;G | snv | 3 | |||
| rs2383205 | 0.925 | 0.080 | 9 | 22060936 | intron variant | A/C;G | snv | 3 | |||
| rs4149310 | 9 | 104826853 | intron variant | A/T | snv | 0.34 | 3 | ||||
| rs4788815 | 16 | 71600908 | intergenic variant | A/T | snv | 0.69 | 3 | ||||
| rs6475604 | 0.925 | 0.040 | 9 | 22052735 | intron variant | T/C | snv | 0.72 | 3 | ||
| rs7044859 | 0.925 | 0.080 | 9 | 22018782 | intron variant | T/A | snv | 0.56 | 3 | ||
| rs7859727 | 1.000 | 0.080 | 9 | 22102166 | intron variant | C/T | snv | 0.57 | 3 | ||
| rs1008878 | 1.000 | 0.040 | 9 | 22036113 | non coding transcript exon variant | G/T | snv | 0.71 | 2 | ||
| rs10115049 | 1.000 | 0.040 | 9 | 22032120 | intron variant | A/G | snv | 0.46 | 2 | ||
| rs10217586 | 1.000 | 0.040 | 9 | 22121350 | intron variant | A/T | snv | 0.52 | 2 | ||
| rs10511701 | 9 | 22112600 | intron variant | T/A;C | snv | 2 | |||||
| rs10738606 | 1.000 | 0.040 | 9 | 22088091 | intron variant | A/T | snv | 0.42 | 2 | ||
| rs10757264 | 1.000 | 0.040 | 9 | 22019733 | intron variant | A/G | snv | 0.58 | 2 | ||
| rs10757265 | 1.000 | 0.040 | 9 | 22048860 | intron variant | T/C | snv | 0.49 | 2 | ||
| rs10757267 | 1.000 | 0.040 | 9 | 22052811 | intron variant | G/A;C;T | snv | 2 | |||
| rs10757270 | 1.000 | 0.040 | 9 | 22072720 | intron variant | A/C;G | snv | 0.40 | 2 | ||
| rs10757277 | 1.000 | 0.040 | 9 | 22124451 | intron variant | A/G | snv | 0.40 | 2 | ||
| rs10811641 | 1.000 | 0.040 | 9 | 22014138 | non coding transcript exon variant | C/G | snv | 0.32 | 2 | ||
| rs10811643 | 1.000 | 0.040 | 9 | 22024967 | intron variant | A/G | snv | 0.56 | 2 |