| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs2256175 | 1.000 | 6 | 31412672 | intron variant | C/T | snv | 0.55 | 5 | |||
| rs2596542 | 0.724 | 0.200 | 6 | 31398818 | upstream gene variant | C/T | snv | 0.41 | 5 | ||
| rs1051794 | 0.925 | 0.120 | 6 | 31411332 | missense variant | G/A | snv | 0.34 | 0.35 | 4 | |
| rs6910087 | 1.000 | 6 | 31409270 | intron variant | C/T | snv | 0.20 | 4 | |||
| rs9266825 | 1.000 | 6 | 31415105 | 3 prime UTR variant | C/A;T | snv | 0.31; 8.1E-06 | 4 | |||
| rs2523454 | 0.882 | 0.240 | 6 | 31400088 | 5 prime UTR variant | G/A | snv | 0.22 | 2 | ||
| rs2256028 | 1.000 | 0.120 | 6 | 31411421 | non coding transcript exon variant | C/A | snv | 0.18 | 1 | ||
| rs9357133 | 1.000 | 0.120 | 6 | 31413120 | intron variant | C/T | snv | 5.3E-02 | 1 | ||
| rs12174396 | 1.000 | 0.120 | 6 | 31406802 | intron variant | A/G | snv | 7.6E-02 | 1 | ||
| rs3763288 | 0.925 | 0.160 | 6 | 31402590 | non coding transcript exon variant | G/A | snv | 5.3E-02 | 1 | ||
| rs9380254 | 1.000 | 0.120 | 6 | 31410558 | missense variant | G/A;C | snv | 5.7E-05; 7.8E-02 | 1 | ||
| rs1063635 | 1.000 | 0.120 | 6 | 31412154 | missense variant | G/A | snv | 0.50 | 0.54 | 1 | |
| rs3094584 | 1.000 | 0.200 | 6 | 31416071 | intron variant | G/A;T | snv | 0.17 | 1 | ||
| rs2256183 | 6 | 31412752 | intron variant | A/G;T | snv | 1 | |||||
| rs6906175 | 6 | 31403324 | intron variant | G/C | snv | 0.31 | 1 | ||||
| rs2252223 | 6 | 31403744 | intron variant | T/C | snv | 7.8E-02 | 0.10 | 1 | |||
| rs2844523 | 6 | 31400811 | intron variant | G/A | snv | 0.10 | 1 |