| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs25487 | 0.441 | 0.800 | 19 | 43551574 | missense variant | T/C | snv | 0.68 | 0.71 | 205 | |
| rs2790457 | 1.000 | 0.160 | 10 | 28567890 | intron variant | G/A | snv | 0.35 | 1 | ||
| rs2010963 | 0.542 | 0.840 | 6 | 43770613 | 5 prime UTR variant | C/G | snv | 0.68 | 82 | ||
| rs699947 | 0.570 | 0.680 | 6 | 43768652 | upstream gene variant | A/C;T | snv | 67 | |||
| rs3025039 | 0.576 | 0.720 | 6 | 43784799 | 3 prime UTR variant | C/T | snv | 0.13 | 62 | ||
| rs2228570 | 0.521 | 0.760 | 12 | 47879112 | start lost | A/C;G;T | snv | 0.63 | 99 | ||
| rs6919908 | 0.882 | 0.160 | 6 | 31277183 | non coding transcript exon variant | T/C | snv | 0.83 | 3 | ||
| rs2272006 | 1.000 | 0.160 | 3 | 41955567 | non coding transcript exon variant | C/T | snv | 0.67 | 1 | ||
| rs2625667 | 1.000 | 0.160 | 3 | 41859459 | non coding transcript exon variant | C/A | snv | 0.32 | 1 | ||
| rs3774372 | 1.000 | 0.160 | 3 | 41835922 | missense variant | T/C | snv | 0.17 | 0.18 | 4 | |
| rs6763508 | 0.851 | 0.160 | 3 | 41709497 | intron variant | T/C | snv | 0.30 | 4 | ||
| rs7372217 | 1.000 | 0.160 | 3 | 41948630 | intron variant | G/A | snv | 0.68 | 4 | ||
| rs7651190 | 1.000 | 0.160 | 3 | 41724463 | intron variant | A/G | snv | 0.33 | 4 | ||
| rs9815354 | 0.925 | 0.160 | 3 | 41871159 | intron variant | G/A;T | snv | 4 | |||
| rs1716983 | 1.000 | 0.160 | 3 | 41922636 | intron variant | G/A;C;T | snv | 3 | |||
| rs1717027 | 1.000 | 0.160 | 3 | 41946428 | intron variant | T/A;C | snv | 3 | |||
| rs73071352 | 0.882 | 0.160 | 3 | 41786808 | intron variant | A/G | snv | 0.12 | 3 | ||
| rs73081364 | 1.000 | 0.160 | 3 | 41872124 | intron variant | G/A;C;T | snv | 3 | |||
| rs7622665 | 1.000 | 0.160 | 3 | 41929251 | intron variant | T/C | snv | 0.67 | 3 | ||
| rs9848754 | 0.882 | 0.160 | 3 | 41712155 | intron variant | C/T | snv | 0.18 | 3 | ||
| rs1052501 | 0.925 | 0.160 | 3 | 41883906 | missense variant | C/G;T | snv | 0.80 | 2 | ||
| rs2272007 | 1.000 | 0.160 | 3 | 41954644 | missense variant | T/C | snv | 0.79 | 0.67 | 2 | |
| rs2683696 | 1.000 | 0.160 | 3 | 41873406 | intron variant | T/C | snv | 0.34 | 2 | ||
| rs28581706 | 1.000 | 0.160 | 3 | 41829905 | intron variant | A/C;T | snv | 2 | |||
| rs62258655 | 1.000 | 0.160 | 3 | 41890838 | intron variant | G/A | snv | 0.11 | 2 |