| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs776270017 | 1.000 | 0.080 | 10 | 90920283 | synonymous variant | T/C | snv | 8.0E-06 | 1 | ||
| rs777551553 | 1.000 | 0.080 | 19 | 44906639 | stop gained | G/A | snv | 4.0E-06 | 1 | ||
| rs747355134 | 1.000 | 0.080 | 21 | 26090027 | missense variant | G/A | snv | 4.0E-06 | 1 | ||
| rs4879628 | 1.000 | 0.080 | 9 | 32888522 | intron variant | T/C | snv | 0.82 | 1 | ||
| rs1298691127 | 1.000 | 0.080 | X | 67711447 | missense variant | G/C | snv | 6.2E-06 | 1 | ||
| rs12651329 | 1.000 | 0.080 | 4 | 36077972 | intron variant | T/C | snv | 0.46 | 1 | ||
| rs2364403 | 1.000 | 0.080 | 1 | 155957961 | intron variant | G/A | snv | 0.25 | 1 | ||
| rs755836362 | 1.000 | 0.080 | 13 | 111267576 | frameshift variant | G/- | delins | 1 | |||
| rs772912273 | 1.000 | 0.080 | 13 | 111209877 | missense variant | G/A | snv | 4.0E-06 | 1 | ||
| rs748086058 | 1.000 | 0.080 | 13 | 111115619 | synonymous variant | G/A;C | snv | 5.7E-06 | 1 | ||
| rs1194556417 | 1.000 | 0.080 | 17 | 33292023 | synonymous variant | C/T | snv | 7.1E-06 | 1 | ||
| rs752612830 | 1.000 | 0.080 | 6 | 106316116 | synonymous variant | T/C | snv | 8.0E-06 | 4.9E-05 | 1 | |
| rs779467346 | 1.000 | 0.080 | 13 | 112785188 | synonymous variant | G/A | snv | 1.3E-05 | 7.0E-06 | 1 | |
| rs1250700280 | 1.000 | 0.080 | 12 | 111525290 | missense variant | C/T | snv | 1 | |||
| rs374385876 | 1.000 | 0.080 | 12 | 111525287 | missense variant | T/C | snv | 4.1E-06 | 3.5E-05 | 1 | |
| rs10143310 | 1.000 | 0.080 | 14 | 92074037 | intron variant | G/A;C | snv | 1 | |||
| rs10438933 | 1.000 | 0.080 | 18 | 31693166 | intergenic variant | A/G | snv | 0.14 | 1 | ||
| rs1409340420 | 1.000 | 0.080 | 20 | 31722126 | synonymous variant | T/C | snv | 7.0E-06 | 1 | ||
| rs1355281868 | 1.000 | 0.080 | 2 | 70214484 | missense variant | A/G | snv | 1 | |||
| rs10122902 | 1.000 | 0.080 | 9 | 27556782 | synonymous variant | G/A | snv | 0.24 | 0.21 | 1 | |
| rs10757665 | 1.000 | 0.080 | 9 | 27557921 | intron variant | T/C | snv | 0.20 | 1 | ||
| rs12349820 | 1.000 | 0.080 | 9 | 27553878 | intron variant | T/C | snv | 0.20 | 1 | ||
| rs1565948 | 1.000 | 0.080 | 9 | 27559735 | non coding transcript exon variant | G/A | snv | 0.43 | 1 | ||
| rs2282240 | 1.000 | 0.080 | 9 | 27572636 | intron variant | C/T | snv | 0.23 | 1 | ||
| rs2282241 | 1.000 | 0.080 | 9 | 27572257 | intron variant | C/A | snv | 0.38 | 1 |