| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs2869966 | 1.000 | 0.040 | 4 | 88947927 | intron variant | C/T | snv | 0.47 | 9 | ||
| rs34811474 | 1.000 | 0.040 | 4 | 25407216 | missense variant | G/A;T | snv | 0.15; 4.1E-06 | 8 | ||
| rs34712979 | 1.000 | 0.040 | 4 | 105897896 | splice region variant | G/A;T | snv | 0.17 | 5 | ||
| rs1250248 | 1.000 | 0.040 | 2 | 215422370 | intron variant | A/G | snv | 0.77 | 4 | ||
| rs1991556 | 1.000 | 0.040 | 17 | 46006036 | intron variant | G/A | snv | 0.14 | 4 | ||
| rs4252548 | 1.000 | 0.040 | 19 | 55368304 | missense variant | C/T | snv | 2.1E-02 | 1.8E-02 | 4 | |
| rs4337252 | 1.000 | 0.040 | 15 | 73934424 | intron variant | G/C | snv | 0.52 | 4 | ||
| rs8042849 | 1.000 | 0.040 | 15 | 78525587 | intron variant | C/T | snv | 0.65 | 4 | ||
| rs8089865 | 1.000 | 0.040 | 18 | 53431552 | intron variant | G/A;C | snv | 4 | |||
| rs199525 | 1.000 | 0.080 | 17 | 46770468 | intron variant | T/A;G | snv | 3 | |||
| rs2290846 | 1.000 | 0.040 | 4 | 150277928 | missense variant | G/A | snv | 0.20 | 0.18 | 3 | |
| rs2555019 | 1.000 | 0.040 | 12 | 114230813 | intergenic variant | T/C;G | snv | 3 | |||
| rs3764002 | 1.000 | 0.080 | 12 | 108224853 | missense variant | C/T | snv | 0.27 | 0.20 | 3 | |
| rs4073153 | 1.000 | 0.200 | 9 | 136364897 | non coding transcript exon variant | A/G | snv | 0.40 | 3 | ||
| rs4642101 | 1.000 | 0.080 | 3 | 12800724 | intron variant | T/G | snv | 0.63 | 3 | ||
| rs7838717 | 1.000 | 0.120 | 8 | 144280310 | intron variant | C/T | snv | 0.30 | 3 | ||
| rs11759026 | 1.000 | 0.080 | 6 | 126470949 | intron variant | A/G | snv | 0.22 | 2 | ||
| rs11762469 | 1.000 | 0.080 | 7 | 140914412 | intron variant | A/G;T | snv | 2 | |||
| rs1490265 | 1.000 | 0.040 | 3 | 67401619 | intron variant | C/A | snv | 0.74 | 2 | ||
| rs62259026 | 1.000 | 0.040 | 3 | 57760788 | intron variant | C/A;T | snv | 2 | |||
| rs6440008 | 1.000 | 0.080 | 3 | 141435700 | intron variant | T/C | snv | 0.42 | 2 | ||
| rs6658835 | 1.000 | 1 | 218347653 | intron variant | A/C;G | snv | 0.39 | 2 | |||
| rs6951144 | 1.000 | 0.080 | 7 | 18872166 | intron variant | C/G | snv | 0.48 | 2 | ||
| rs7571971 | 1.000 | 0.120 | 2 | 88595833 | non coding transcript exon variant | T/C | snv | 0.70 | 0.77 | 2 | |
| rs9350191 | 1.000 | 0.040 | 6 | 19842430 | upstream gene variant | C/G;T | snv | 2 |