| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs2077777 | 1.000 | 0.120 | 4 | 26322296 | splice region variant | G/C | snv | 8.9E-02 | 1 | ||
| rs2270226 | 1.000 | 0.120 | 4 | 26415514 | missense variant | T/A;C;G | snv | 0.57 | 1 | ||
| rs2271875 | 1.000 | 0.120 | 19 | 3626924 | upstream gene variant | T/C | snv | 0.68 | 1 | ||
| rs2275235 | 1.000 | 0.120 | 1 | 150757803 | intron variant | A/G | snv | 0.34 | 1 | ||
| rs35364374 | 1.000 | 0.120 | 19 | 38492540 | missense variant | G/T | snv | 6.9E-02 | 5.0E-02 | 1 | |
| rs4382936 | 1.000 | 0.120 | 11 | 73241355 | non coding transcript exon variant | A/C | snv | 0.36 | 1 | ||
| rs4769055 | 1.000 | 0.120 | 13 | 30735693 | intron variant | C/A | snv | 0.41 | 0.47 | 1 | |
| rs4806942 | 1.000 | 0.120 | 19 | 3589341 | intron variant | G/A | snv | 0.13 | 1 | ||
| rs4919862 | 1.000 | 0.120 | 19 | 582253 | intron variant | T/C | snv | 0.82 | 1 | ||
| rs4944832 | 1.000 | 0.120 | 11 | 73238127 | upstream gene variant | G/A;T | snv | 1 | |||
| rs494860 | 1.000 | 0.120 | 13 | 113164695 | intron variant | T/A | snv | 0.26 | 0.19 | 1 | |
| rs56095120 | 1.000 | 0.120 | 22 | 31100540 | intron variant | T/A;C | snv | 1 | |||
| rs5997872 | 1.000 | 0.120 | 22 | 31095346 | missense variant | C/T | snv | 0.14 | 0.16 | 1 | |
| rs7042521 | 1.000 | 0.120 | 9 | 137889440 | intron variant | C/G | snv | 0.31 | 1 | ||
| rs755403632 | 1.000 | 0.120 | 10 | 42792991 | missense variant | C/G;T | snv | 4.0E-06; 4.0E-06 | 1 | ||
| rs774320676 | 1.000 | 0.120 | 1 | 150750091 | missense variant | A/T | snv | 4.0E-06 | 1 | ||
| rs928508030 | 1.000 | 0.120 | 1 | 150765698 | splice region variant | G/A | snv | 1 | |||
| rs9621187 | 1.000 | 0.120 | 22 | 31103532 | non coding transcript exon variant | A/G | snv | 0.35 | 1 | ||
| rs10846744 | 0.763 | 0.160 | 12 | 124827879 | intron variant | G/C | snv | 0.32 | 11 | ||
| rs2106261 | 0.763 | 0.160 | 16 | 73017721 | intron variant | C/G;T | snv | 11 | |||
| rs2066715 | 0.807 | 0.160 | 9 | 104825752 | missense variant | C/T | snv | 8.2E-02 | 5.5E-02 | 7 | |
| rs3861950 | 0.827 | 0.160 | 1 | 173187153 | intron variant | T/C | snv | 0.47 | 7 | ||
| rs619203 | 0.851 | 0.160 | 6 | 117301021 | missense variant | G/C | snv | 0.20 | 0.19 | 6 | |
| rs774229224 | 0.882 | 0.160 | 6 | 160706454 | missense variant | C/A;G | snv | 4.0E-06; 4.0E-06 | 6 | ||
| rs9551963 | 0.851 | 0.160 | 13 | 30758410 | intron variant | A/C;T | snv | 6 |