| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs17135889 | 0.925 | 0.080 | 16 | 2337259 | intron variant | G/A | snv | 0.11 | 2 | ||
| rs35768389 | 0.925 | 0.160 | 2 | 11214974 | missense variant | T/A | snv | 3.5E-04 | 3.6E-04 | 2 | |
| rs170447 | 1.000 | 0.080 | 16 | 2299370 | intron variant | T/C | snv | 0.51 | 0.45 | 1 | |
| rs1923537 | 1.000 | 0.080 | 10 | 79935452 | intron variant | A/G | snv | 0.37 | 1 | ||
| rs2271255 | 1.000 | 0.080 | 18 | 21044113 | missense variant | T/C | snv | 3.6E-05 | 7.0E-06 | 1 | |
| rs313909 | 1.000 | 0.080 | 16 | 2287992 | intron variant | G/A;C | snv | 0.42; 4.3E-06 | 1 | ||
| rs323043 | 1.000 | 0.080 | 16 | 2298527 | synonymous variant | G/A;C;T | snv | 8.0E-06; 0.14; 4.0E-06 | 1 | ||
| rs370068089 | 1.000 | 0.080 | 8 | 22164041 | stop lost | G/C | snv | 5.6E-05 | 1 | ||
| rs531292167 | 1.000 | 0.080 | 18 | 21006431 | missense variant | T/A | snv | 4.0E-06 | 1 | ||
| rs726843 | 1.000 | 0.080 | 2 | 11216064 | intron variant | G/A | snv | 0.38 | 1 | ||
| rs7956915 | 1.000 | 0.080 | 12 | 6361094 | intron variant | A/G | snv | 0.52 | 1 | ||
| rs952222278 | 1.000 | 0.080 | 7 | 87550238 | missense variant | T/C | snv | 4.0E-06 | 7.0E-06 | 1 |