| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs266851 | 0.882 | 0.120 | 19 | 50833083 | intron variant | C/T | snv | 0.20 | 3 | ||
| rs4320932 | 0.882 | 0.120 | 11 | 2150371 | intron variant | T/C | snv | 0.19 | 3 | ||
| rs4648551 | 0.882 | 0.120 | 1 | 3716166 | intron variant | G/A | snv | 0.32 | 3 | ||
| rs567534295 | 0.882 | 0.120 | 17 | 43048090 | intron variant | C/T | snv | 2.8E-05 | 3 | ||
| rs6695978 | 0.882 | 0.120 | 1 | 3731781 | intron variant | G/A | snv | 7.3E-02 | 3 | ||
| rs759920 | 0.882 | 0.120 | 19 | 10174102 | intron variant | A/G;T | snv | 3 | |||
| rs7650365 | 0.882 | 0.120 | 3 | 128115160 | intron variant | G/A | snv | 0.35 | 3 | ||
| rs7651446 | 0.882 | 0.120 | 3 | 156689208 | intron variant | G/T | snv | 7.9E-02 | 3 | ||
| rs7727832 | 0.882 | 0.120 | 5 | 142611975 | intron variant | C/T | snv | 0.10 | 3 | ||
| rs9303542 | 0.882 | 0.120 | 17 | 48334138 | intron variant | A/G | snv | 0.34 | 3 | ||
| rs34289250 | 0.925 | 0.120 | 17 | 61803285 | intron variant | T/C | snv | 7.8E-03 | 2 | ||
| rs367899983 | 1.000 | 0.120 | 9 | 16864524 | intron variant | GTCT/- | delins | 4.2E-05 | 2 | ||
| rs10756819 | 1.000 | 0.120 | 9 | 16858086 | intron variant | G/A;C;T | snv | 1 | |||
| rs12379183 | 1.000 | 0.120 | 9 | 16865701 | intron variant | A/G | snv | 0.26 | 1 | ||
| rs12379687 | 1.000 | 0.120 | 9 | 16854369 | intron variant | G/A;T | snv | 1 | |||
| rs12451939 | 1.000 | 0.120 | 17 | 61970281 | intron variant | A/G | snv | 2.6E-02 | 1 | ||
| rs12937080 | 1.000 | 0.120 | 17 | 61852376 | intron variant | A/G;T | snv | 1 | |||
| rs12938171 | 1.000 | 0.120 | 17 | 61902994 | intron variant | G/A | snv | 9.0E-03 | 1 | ||
| rs1339552 | 1.000 | 0.120 | 9 | 16848792 | intron variant | C/T | snv | 0.52 | 1 | ||
| rs1416742 | 1.000 | 0.120 | 9 | 16856885 | intron variant | G/A | snv | 0.43 | 1 | ||
| rs4961501 | 1.000 | 0.120 | 9 | 16851680 | intron variant | T/A;C;G | snv | 1 | |||
| rs7861573 | 1.000 | 0.120 | 9 | 16862282 | intron variant | A/G;T | snv | 1 | |||
| rs2660753 | 0.790 | 0.240 | 3 | 87061524 | intergenic variant | T/C | snv | 0.76 | 9 | ||
| rs7313833 | 0.851 | 0.120 | 12 | 27930263 | intergenic variant | G/A | snv | 0.37 | 4 | ||
| rs7365052 | 0.882 | 0.120 | 1 | 236786561 | intergenic variant | T/C | snv | 3 |