| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs12740374 | 0.851 | 0.040 | 1 | 109274968 | 3 prime UTR variant | G/T | snv | 0.22 | 16 | ||
| rs61776719 | 0.776 | 0.120 | 1 | 37995647 | downstream gene variant | C/A | snv | 0.46 | 11 | ||
| rs11205303 | 0.882 | 0.120 | 1 | 149934520 | missense variant | T/C | snv | 0.33 | 0.29 | 9 | |
| rs34517439 | 0.882 | 0.120 | 1 | 77984833 | intron variant | C/A | snv | 7.3E-02 | 7 | ||
| rs17391694 | 0.882 | 0.120 | 1 | 78157942 | regulatory region variant | C/T | snv | 7.8E-02 | 6 | ||
| rs2284746 | 1 | 16980180 | intron variant | C/A;G | snv | 6 | |||||
| rs11205277 | 1.000 | 0.120 | 1 | 149920979 | upstream gene variant | A/C;G;T | snv | 5 | |||
| rs114165349 | 1 | 26695422 | intron variant | G/C | snv | 1.7E-02 | 5 | ||||
| rs2274432 | 1 | 184051811 | missense variant | G/A | snv | 0.33 | 0.28 | 5 | |||
| rs1046934 | 1.000 | 0.080 | 1 | 184054395 | missense variant | A/C;G;T | snv | 0.34; 4.0E-06 | 4 | ||
| rs34720381 | 1 | 171486183 | intron variant | C/T | snv | 7.3E-02 | 4 | ||||
| rs1149048 | 0.925 | 0.200 | 1 | 30725886 | non coding transcript exon variant | A/C;G | snv | 3 | |||
| rs1890995 | 1 | 218431336 | intron variant | G/A | snv | 0.33 | 3 | ||||
| rs28673728 | 1 | 37943401 | intron variant | A/G | snv | 0.40 | 3 | ||||
| rs3738814 | 1 | 17005181 | intron variant | A/G | snv | 0.52 | 3 | ||||
| rs3795503 | 1 | 180936558 | synonymous variant | C/T | snv | 0.31 | 0.27 | 3 | |||
| rs3814333 | 1 | 184037985 | upstream gene variant | C/T | snv | 0.29 | 3 | ||||
| rs6684205 | 1 | 218436360 | intron variant | A/G;T | snv | 3 | |||||
| rs7534091 | 1 | 118321993 | intergenic variant | A/G | snv | 0.23 | 3 | ||||
| rs823118 | 0.925 | 0.080 | 1 | 205754444 | upstream gene variant | C/A;T | snv | 3 | |||
| rs9435733 | 1 | 16981759 | intron variant | T/C | snv | 0.41 | 3 | ||||
| rs1044299 | 1 | 176842737 | 3 prime UTR variant | C/G;T | snv | 2 | |||||
| rs10482795 | 1 | 218432267 | intron variant | G/A;T | snv | 2 | |||||
| rs10799445 | 1 | 227724182 | upstream gene variant | A/C | snv | 0.27 | 2 | ||||
| rs10863936 | 1 | 212064456 | intron variant | G/A | snv | 0.59 | 2 |