| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs1042718 | 0.925 | 0.080 | 5 | 148827354 | missense variant | C/A;T | snv | 0.23; 4.0E-06 | 3 | ||
| rs480902 | 0.882 | 0.200 | 1 | 231395881 | intron variant | T/C | snv | 0.64 | 3 | ||
| rs72625676 | 0.882 | 0.120 | 14 | 69307268 | intron variant | C/T | snv | 6.3E-02 | 3 | ||
| rs6089953 | 0.882 | 0.080 | 20 | 63659655 | intron variant | A/G | snv | 0.82 | 3 | ||
| rs539689 | 0.925 | 0.080 | 6 | 31829810 | synonymous variant | C/G | snv | 0.57 | 0.52 | 2 | |
| rs199983 | 1.000 | 0.040 | 6 | 104412396 | intergenic variant | A/G | snv | 0.52 | 1 | ||
| rs4461142 | 1.000 | 0.040 | 17 | 63500687 | intron variant | T/C | snv | 0.62 | 1 | ||
| rs8066114 | 1.000 | 0.040 | 17 | 63512479 | intron variant | C/G | snv | 0.36 | 1 | ||
| rs843752 | 1.000 | 0.040 | 2 | 54219450 | intron variant | T/A;G | snv | 1 | |||
| rs749174 | 1.000 | 0.040 | 11 | 67585782 | intron variant | G/A | snv | 0.29 | 1 | ||
| rs157928 | 1.000 | 0.040 | 7 | 130896599 | intron variant | T/C | snv | 0.29 | 1 | ||
| rs1962430 | 1.000 | 0.040 | 8 | 9902110 | non coding transcript exon variant | G/A;C;T | snv | 1 | |||
| rs2272026 | 1.000 | 0.040 | 8 | 9900090 | non coding transcript exon variant | C/G;T | snv | 1 | |||
| rs2918417 | 1.000 | 0.040 | 5 | 143346605 | intron variant | C/T | snv | 0.29 | 1 | ||
| rs4634384 | 1.000 | 0.040 | 5 | 143401132 | intron variant | C/T | snv | 0.52 | 1 | ||
| rs6188 | 1.000 | 0.040 | 5 | 143300779 | intron variant | C/A | snv | 0.26 | 0.29 | 1 | |
| rs6194 | 1.000 | 0.040 | 5 | 143298796 | synonymous variant | G/A | snv | 8.4E-03 | 3.9E-03 | 1 | |
| rs4963516 | 1.000 | 0.040 | 12 | 6838864 | intron variant | T/G | snv | 0.15 | 1 | ||
| rs6010621 | 1.000 | 0.040 | 20 | 63679519 | intron variant | T/G | snv | 0.81 | 1 | ||
| rs130293 | 1.000 | 0.040 | 22 | 32825953 | intron variant | G/A | snv | 0.92 | 1 |