| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs7085433 | 1.000 | 0.040 | 10 | 46002468 | intron variant | C/T | snv | 9.5E-02 | 4 | ||
| rs12492609 | 0.882 | 0.040 | 3 | 119435715 | intron variant | C/T | snv | 0.14 | 3 | ||
| rs1537424 | 1.000 | 0.040 | 14 | 36104812 | intron variant | C/T | snv | 0.49 | 3 | ||
| rs7629750 | 0.882 | 0.040 | 3 | 119455829 | intron variant | A/G | snv | 0.45 | 3 | ||
| rs11935941 | 1.000 | 0.040 | 4 | 148731326 | intron variant | A/C | snv | 0.31 | 2 | ||
| rs2056252 | 1.000 | 0.040 | 4 | 165026338 | non coding transcript exon variant | G/A | snv | 0.16 | 2 | ||
| rs2227478 | 0.925 | 0.040 | 12 | 68254842 | upstream gene variant | A/G | snv | 0.37 | 2 | ||
| rs6972286 | 1.000 | 0.040 | 7 | 118685680 | intergenic variant | A/T | snv | 0.43 | 2 | ||
| rs7178239 | 1.000 | 0.040 | 15 | 101267907 | downstream gene variant | C/G | snv | 0.37 | 2 | ||
| rs756763 | 1.000 | 0.040 | 17 | 51671952 | intron variant | A/G | snv | 0.48 | 2 | ||
| rs977706 | 1.000 | 0.040 | 17 | 13456118 | intergenic variant | A/T | snv | 0.13 | 2 | ||
| rs12507813 | 1.000 | 0.040 | 4 | 165013422 | upstream gene variant | G/A;C;T | snv | 1 | |||
| rs12551356 | 1.000 | 0.040 | 9 | 74698280 | intergenic variant | G/T | snv | 0.11 | 1 | ||
| rs12730735 | 1.000 | 0.040 | 1 | 113838835 | intron variant | T/C | snv | 0.21 | 1 | ||
| rs12944194 | 1.000 | 0.040 | 17 | 73850424 | intergenic variant | T/C | snv | 0.63 | 1 | ||
| rs165501 | 1.000 | 0.040 | 3 | 10167559 | intron variant | T/A;C | snv | 1 | |||
| rs2009895 | 1.000 | 0.040 | 15 | 101276024 | intron variant | C/A;T | snv | 3.0E-02 | 1 | ||
| rs2298213 | 1.000 | 0.040 | 1 | 1203822 | synonymous variant | T/C | snv | 9.1E-02 | 0.17 | 1 | |
| rs3027452 | 1.000 | 0.040 | X | 43798542 | intron variant | G/A | snv | 0.13 | 1 | ||
| rs75201096 | 1.000 | 0.040 | 9 | 77483984 | intron variant | T/C | snv | 1.6E-02 | 1 | ||
| rs791903 | 1.000 | 0.040 | 6 | 33734868 | intron variant | G/C | snv | 0.53 | 1 | ||
| rs9606615 | 1.000 | 0.040 | 22 | 17099923 | intron variant | T/C | snv | 0.41 | 1 | ||
| rs9607715 | 1.000 | 0.040 | 22 | 40399790 | intron variant | G/A | snv | 3.4E-02 | 1 | ||
| rs121434257 | 0.827 | 0.080 | 21 | 44289686 | missense variant | G/A;T | snv | 4.0E-05 | 6 | ||
| rs1133076 | 0.925 | 0.080 | 8 | 133113438 | missense variant | G/A | snv | 0.48 | 0.56 | 2 |