| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs71641308 | 1.000 | 0.080 | 1 | 77621033 | intron variant | C/A;G;T | snv | 1 | |||
| rs67340775 | 1.000 | 0.080 | 6 | 28336607 | intron variant | A/C | snv | 6.3E-02 | 1 | ||
| rs13201681 | 1.000 | 0.080 | 6 | 28426903 | intergenic variant | C/T | snv | 5.0E-02 | 1 | ||
| rs67381177 | 1.000 | 0.080 | 6 | 28444164 | upstream gene variant | G/C;T | snv | 1 | |||
| rs34662244 | 0.925 | 0.120 | 6 | 28106103 | intron variant | G/A | snv | 5.0E-02 | 2 | ||
| rs35952432 | 1.000 | 0.080 | 6 | 28107123 | intron variant | C/T | snv | 5.0E-02 | 1 | ||
| rs9261204 | 0.790 | 0.200 | 6 | 30037466 | intron variant | A/G | snv | 0.17 | 9 | ||
| rs3757328 | 0.851 | 0.120 | 6 | 30060575 | non coding transcript exon variant | G/A | snv | 9.8E-02 | 6 | ||
| rs116480994 | 0.925 | 0.080 | 6 | 30064745 | 3 prime UTR variant | A/C | snv | 2 | |||
| rs17723637 | 0.882 | 0.080 | 9 | 106925122 | missense variant | A/G | snv | 0.14 | 0.13 | 3 | |
| rs760943842 | 0.851 | 0.080 | 1 | 23362976 | missense variant | G/A | snv | 4.0E-05 | 1.4E-05 | 5 | |
| rs115287935 | 1.000 | 0.080 | 6 | 29006488 | upstream gene variant | G/T | snv | 1 | |||
| rs149866169 | 0.925 | 0.080 | 6 | 27473944 | intron variant | T/A;C | snv | 2 | |||
| rs1327135247 | 0.827 | 0.160 | 10 | 31510820 | missense variant | C/T | snv | 4.0E-06 | 5 | ||
| rs1487151044 | 0.851 | 0.080 | 10 | 31510817 | missense variant | T/C | snv | 5 | |||
| rs145204276 | 0.658 | 0.320 | 1 | 173868254 | splice donor variant | CAAGG/- | delins | 8.8E-02 | 31 | ||
| rs3747093 | 0.732 | 0.200 | 22 | 21630090 | upstream gene variant | G/A | snv | 0.32 | 16 | ||
| rs2131877 | 0.827 | 0.080 | 3 | 195137645 | intron variant | G/A | snv | 0.20 | 6 | ||
| rs2025811 | 0.882 | 0.080 | 20 | 21354475 | intron variant | T/C | snv | 0.89 | 3 | ||
| rs5751129 | 0.752 | 0.320 | 22 | 41619761 | intron variant | C/T | snv | 0.69 | 14 | ||
| rs132774 | 0.776 | 0.280 | 22 | 41635949 | intron variant | C/G | snv | 0.69 | 9 | ||
| rs6869366 | 0.701 | 0.280 | 5 | 83075927 | intron variant | T/G | snv | 9.2E-02 | 18 | ||
| rs7727691 | 0.763 | 0.200 | 5 | 83075876 | intron variant | C/T | snv | 0.32 | 9 | ||
| rs1805377 | 0.689 | 0.480 | 5 | 83353124 | splice acceptor variant | G/A | snv | 0.23 | 0.25 | 19 | |
| rs3734091 | 0.689 | 0.280 | 5 | 83204915 | missense variant | G/T | snv | 2.3E-02 | 1.4E-02 | 19 |