| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs11728697 | 0.925 | 0.080 | 4 | 87977789 | non coding transcript exon variant | C/T | snv | 0.54 | 0.46 | 2 | |
| rs3753348 | 0.925 | 0.080 | 1 | 1208277 | upstream gene variant | C/G;T | snv | 2 | |||
| rs2540438 | 1.000 | 0.040 | 2 | 201485833 | downstream gene variant | C/A | snv | 0.29 | 1 | ||
| rs16966671 | 1.000 | 0.040 | 16 | 88651867 | upstream gene variant | C/G | snv | 0.43 | 1 | ||
| rs10502001 | 1.000 | 0.040 | 11 | 102527862 | missense variant | C/G;T | snv | 0.19 | 1 | ||
| rs3748076 | 1.000 | 0.040 | 6 | 143757963 | intron variant | G/A | snv | 0.56 | 1 | ||
| rs2274554 | 1.000 | 0.040 | 13 | 79366394 | intron variant | G/A | snv | 0.40 | 1 | ||
| rs1053411 | 1.000 | 0.040 | 5 | 151663542 | 3 prime UTR variant | G/C;T | snv | 0.21; 4.0E-06 | 1 | ||
| rs1059279 | 1.000 | 0.040 | 5 | 151662618 | 3 prime UTR variant | A/C;T | snv | 0.14 | 1 | ||
| rs1059829 | 1.000 | 0.040 | 5 | 151662468 | 3 prime UTR variant | G/A | snv | 0.45 | 1 | ||
| rs1667614 | 1.000 | 0.040 | 2 | 74121852 | non coding transcript exon variant | A/G;T | snv | 1 | |||
| rs11466668 | 1.000 | 0.040 | 1 | 1207346 | upstream gene variant | G/T | snv | 5.7E-03 | 1 |