| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs2228146 | 0.925 | 0.120 | 1 | 154454574 | missense variant | G/A | snv | 1.3E-02; 4.0E-06 | 5.4E-02 | 3 | |
| rs7222331 | 0.925 | 0.120 | 17 | 40995605 | upstream gene variant | C/T | snv | 0.24 | 3 | ||
| rs758130759 | 0.925 | 0.120 | 17 | 37699149 | missense variant | C/T | snv | 1.6E-05 | 1.4E-05 | 3 | |
| rs11538209 | 1.000 | 0.120 | 4 | 73404356 | missense variant | T/C | snv | 2 | |||
| rs1888747 | 1.000 | 0.120 | 9 | 83540636 | upstream gene variant | C/G | snv | 0.78 | 2 | ||
| rs10019835 | 1.000 | 0.120 | 4 | 155712034 | intron variant | T/A;C | snv | 1 | |||
| rs10047560 | 1.000 | 0.120 | 12 | 20452282 | intron variant | A/G | snv | 0.86 | 1 | ||
| rs1034589 | 1.000 | 0.120 | 22 | 31183247 | intron variant | C/T | snv | 0.79 | 1 | ||
| rs10868025 | 1.000 | 0.120 | 9 | 83549261 | intergenic variant | A/G | snv | 0.30 | 1 | ||
| rs10951509 | 1.000 | 0.120 | 7 | 37173878 | intron variant | G/A;C | snv | 1 | |||
| rs10952362 | 1.000 | 0.120 | 7 | 152565713 | regulatory region variant | T/C | snv | 0.25 | 1 | ||
| rs11107616 | 1.000 | 0.120 | 12 | 77971000 | intron variant | T/G | snv | 0.13 | 1 | ||
| rs11130362 | 1.000 | 0.120 | 3 | 53231750 | non coding transcript exon variant | C/T | snv | 0.24 | 1 | ||
| rs1129456 | 1.000 | 0.120 | 15 | 32734466 | 3 prime UTR variant | A/T | snv | 0.19 | 1 | ||
| rs1157043147 | 1.000 | 0.120 | 17 | 63477150 | missense variant | T/C | snv | 2.8E-05 | 1 | ||
| rs11645214 | 1.000 | 0.120 | 16 | 70575084 | 3 prime UTR variant | A/G | snv | 0.39 | 1 | ||
| rs11886047 | 1.000 | 0.120 | 2 | 43623451 | upstream gene variant | T/A;C | snv | 0.20 | 1 | ||
| rs1249910 | 1.000 | 0.120 | 3 | 112672327 | intergenic variant | A/G | snv | 0.58 | 1 | ||
| rs12523822 | 1.000 | 0.120 | 6 | 154633286 | intergenic variant | C/G;T | snv | 1 | |||
| rs1252906 | 1.000 | 0.120 | 14 | 59192073 | intron variant | A/C;G | snv | 1 | |||
| rs1253192 | 1.000 | 0.120 | 14 | 59376688 | intergenic variant | A/G | snv | 0.92 | 1 | ||
| rs12708815 | 1.000 | 0.120 | 16 | 17134511 | synonymous variant | G/A;C | snv | 0.56 | 1 | ||
| rs1298908 | 1.000 | 0.120 | 10 | 80253378 | non coding transcript exon variant | C/T | snv | 0.48 | 0.53 | 1 | |
| rs13254600 | 1.000 | 0.120 | 8 | 123077286 | intron variant | C/A;G | snv | 0.28; 4.8E-06 | 1 | ||
| rs1341633213 | 1.000 | 0.120 | 17 | 63496422 | stop gained | C/T | snv | 4.0E-06 | 1 |