| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs2179174 | 1.000 | 0.120 | 6 | 28271191 | intron variant | A/G;T | snv | 1 | |||
| rs964184 | 0.716 | 0.440 | 11 | 116778201 | 3 prime UTR variant | G/C | snv | 0.82 | 38 | ||
| rs59716545 | 1.000 | 0.120 | 17 | 39875604 | intron variant | T/G | snv | 0.35 | 1 | ||
| rs166327 | 1.000 | 0.120 | 6 | 30035104 | non coding transcript exon variant | T/C | snv | 0.44 | 1 | ||
| rs4711207 | 1.000 | 0.120 | 6 | 30037977 | intron variant | C/A | snv | 0.23 | 1 | ||
| rs6496667 | 1.000 | 0.120 | 15 | 90350436 | upstream gene variant | C/A;G;T | snv | 1 | |||
| rs1830035 | 1.000 | 0.120 | 7 | 64266267 | missense variant | T/C | snv | 8.2E-02 | 0.12 | 1 | |
| rs2187874 | 1.000 | 0.120 | 4 | 82429 | intron variant | G/T | snv | 0.14 | 1 | ||
| rs2278600 | 1.000 | 0.120 | 5 | 72460843 | missense variant | C/A;G;T | snv | 0.20 | 1 | ||
| rs2290652 | 1.000 | 0.120 | 19 | 34684303 | missense variant | A/G;T | snv | 0.31 | 1 | ||
| rs1543922 | 1.000 | 0.120 | 19 | 51581583 | intron variant | C/T | snv | 0.11 | 1 | ||
| rs11761528 | 1.000 | 0.120 | 7 | 99521178 | intron variant | C/T | snv | 0.12 | 3 | ||
| rs2235359 | 0.925 | 0.160 | 6 | 28247863 | intron variant | T/G | snv | 0.20 | 1 | ||
| rs4809330 | 0.925 | 0.160 | 20 | 63718234 | intron variant | A/G;T | snv | 1 | |||
| rs3129054 | 1.000 | 0.120 | 6 | 29681279 | upstream gene variant | C/T | snv | 0.35 | 1 | ||
| rs9266688 | 1.000 | 0.120 | 6 | 31380766 | non coding transcript exon variant | G/A | snv | 0.14 | 1 | ||
| rs11556924 | 0.752 | 0.240 | 7 | 130023656 | missense variant | C/A;T | snv | 4.0E-06; 0.28 | 14 | ||
| rs2247385 | 1.000 | 0.120 | 6 | 33453800 | intron variant | T/C | snv | 0.42 | 1 | ||
| rs3779381 | 0.925 | 0.160 | 7 | 121326736 | intron variant | A/G | snv | 0.29 | 3 | ||
| rs75908454 | 1.000 | 0.120 | 6 | 169570527 | intron variant | T/C | snv | 4.6E-02 | 1 | ||
| rs2671692 | 1.000 | 0.120 | 10 | 48889774 | intron variant | G/A | snv | 0.54 | 1 | ||
| rs7097397 | 0.925 | 0.120 | 10 | 48817351 | missense variant | G/A | snv | 0.38 | 0.31 | 1 | |
| rs707928 | 0.827 | 0.320 | 6 | 31774813 | intron variant | A/G | snv | 0.47 | 4 | ||
| rs707929 | 1.000 | 0.120 | 6 | 31774290 | intron variant | A/G | snv | 0.46 | 1 | ||
| rs213199 | 1.000 | 0.120 | 6 | 33267978 | synonymous variant | G/A | snv | 0.39 | 0.40 | 1 |