| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs13107325 | 0.776 | 0.520 | 4 | 102267552 | missense variant | C/A;T | snv | 4.0E-06; 4.5E-02 | 34 | ||
| rs2239647 | 0.851 | 0.080 | 14 | 32823537 | synonymous variant | A/C | snv | 0.60 | 0.65 | 7 | |
| rs13212562 | 0.925 | 0.120 | 6 | 27332531 | intergenic variant | A/G | snv | 0.13 | 4 | ||
| rs6704768 | 1.000 | 0.040 | 2 | 232727791 | intron variant | G/A | snv | 0.54 | 4 | ||
| rs10752262 | 1.000 | 0.040 | 10 | 12353101 | intron variant | C/T | snv | 0.39 | 3 | ||
| rs11765189 | 1.000 | 0.040 | 7 | 157743285 | intron variant | A/G | snv | 0.25 | 3 | ||
| rs12602286 | 1.000 | 0.040 | 17 | 19333641 | intron variant | G/T | snv | 0.79 | 3 | ||
| rs3747631 | 1.000 | 0.040 | 1 | 204618441 | missense variant | G/A;C | snv | 4.0E-06; 0.20 | 3 | ||
| rs62154720 | 1.000 | 0.040 | 2 | 105306623 | intron variant | C/T | snv | 9.2E-02 | 3 | ||
| rs76076331 | 1.000 | 0.040 | 2 | 10837459 | intron variant | C/T | snv | 1.0E-01 | 3 | ||
| rs78381888 | 0.925 | 0.040 | 2 | 96835038 | 3 prime UTR variant | A/G | snv | 0.13 | 3 | ||
| rs9556958 | 1.000 | 0.040 | 13 | 98447792 | 3 prime UTR variant | C/G;T | snv | 3 | |||
| rs9616914 | 1.000 | 0.040 | 22 | 50678709 | intron variant | G/A | snv | 0.35 | 0.36 | 3 | |
| rs10098073 | 1.000 | 0.040 | 8 | 142228143 | intron variant | C/A | snv | 0.35 | 2 | ||
| rs13217239 | 1.000 | 0.040 | 6 | 27287188 | intron variant | T/C | snv | 0.39 | 2 | ||
| rs165655 | 1.000 | 0.040 | 22 | 19970240 | 3 prime UTR variant | G/A | snv | 0.56 | 2 | ||
| rs589249 | 1.000 | 0.040 | 1 | 36696751 | intergenic variant | A/G;T | snv | 2 | |||
| rs67575965 | 1.000 | 0.040 | 6 | 26196365 | 3 prime UTR variant | A/G | snv | 0.21 | 2 | ||
| rs73219805 | 1.000 | 0.040 | 8 | 26415252 | intron variant | G/A | snv | 0.19 | 2 |