| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs2523987 | 0.827 | 0.280 | 6 | 30112216 | intron variant | A/C | snv | 9.2E-02 | 5 | ||
| rs2844795 | 0.925 | 0.120 | 6 | 30106070 | intron variant | C/G;T | snv | 5 | |||
| rs2523989 | 0.827 | 0.280 | 6 | 30110498 | missense variant | C/T | snv | 0.12 | 0.12 | 4 | |
| rs2517598 | 0.851 | 0.280 | 6 | 30112497 | synonymous variant | G/A | snv | 0.14 | 0.13 | 4 | |
| rs4959041 | 0.925 | 0.120 | 6 | 30110190 | intron variant | T/C | snv | 0.29 | 2 | ||
| rs3132680 | 1.000 | 0.120 | 6 | 30105418 | non coding transcript exon variant | A/C | snv | 0.73 | 1 | ||
| rs2523990 | 1.000 | 0.120 | 6 | 30109452 | intron variant | A/G | snv | 0.43 | 1 | ||
| rs11964542 | 1.000 | 0.040 | 6 | 30103983 | non coding transcript exon variant | T/C | snv | 7.2E-02 | 1 | ||
| rs2023472 | 6 | 30108087 | missense variant | A/C;G | snv | 4.1E-06; 0.68 | 1 |