| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| 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 | ||
| rs10811645 | 1.000 | 0.040 | 9 | 22049657 | intron variant | G/A | snv | 0.59 | 2 | ||
| rs10811651 | 1.000 | 0.040 | 9 | 22067831 | intron variant | G/A;C | snv | 2 | |||
| rs10965224 | 1.000 | 0.040 | 9 | 22067277 | intron variant | T/A | snv | 0.64 | 2 | ||
| rs1333036 | 1.000 | 0.040 | 9 | 22043820 | intron variant | T/C | snv | 0.58 | 2 | ||
| rs1333039 | 1.000 | 0.040 | 9 | 22065658 | splice region variant | G/A;C;T | snv | 2 | |||
| rs1333043 | 9 | 22106732 | intron variant | T/A | snv | 0.64 | 2 | ||||
| rs1360589 | 1.000 | 0.040 | 9 | 22045318 | intron variant | C/T | snv | 0.72 | 2 | ||
| rs1360590 | 1.000 | 0.040 | 9 | 22041444 | intron variant | T/C;G | snv | 2 | |||
| rs1537370 | 1.000 | 9 | 22084311 | intron variant | C/T | snv | 0.55 | 2 | |||
| rs1537376 | 1.000 | 0.040 | 9 | 22116221 | intron variant | T/C | snv | 0.49 | 2 | ||
| rs1556515 | 1.000 | 0.040 | 9 | 22036368 | non coding transcript exon variant | C/T | snv | 0.71 | 2 | ||
| rs2106119 | 1.000 | 0.040 | 9 | 22017551 | intron variant | A/G;T | snv | 2 | |||
| rs2106120 | 1.000 | 0.040 | 9 | 22017102 | intron variant | G/T | snv | 0.56 | 2 | ||
| rs2184061 | 1.000 | 0.040 | 9 | 22061563 | intron variant | C/A;T | snv | 0.64 | 2 | ||
| rs4977575 | 1.000 | 0.040 | 9 | 22124745 | intron variant | C/G;T | snv | 2 | |||
| rs4977753 | 1.000 | 0.040 | 9 | 22030028 | non coding transcript exon variant | C/T | snv | 0.58 | 2 | ||
| rs543830 | 1.000 | 0.040 | 9 | 22026640 | intron variant | A/C;T | snv | 2 | |||
| rs6475608 | 1.000 | 0.080 | 9 | 22101703 | intron variant | T/C | snv | 0.60 | 2 |