| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs16970006 | 1.000 | 0.040 | 15 | 78677917 | intron variant | T/C | snv | 8.7E-02 | 2 | ||
| rs3885951 | 1.000 | 0.040 | 15 | 78533575 | missense variant | A/G | snv | 7.5E-02 | 6.9E-02 | 2 | |
| rs12503223 | 1.000 | 0.040 | 4 | 16841093 | intron variant | G/A | snv | 0.18 | 1 | ||
| rs2495239 | 1.000 | 0.040 | 6 | 41522750 | intron variant | A/G | snv | 0.84 | 1 | ||
| rs6988624 | 1.000 | 0.040 | 8 | 64019391 | intron variant | C/A;T | snv | 1 | |||
| rs7216064 | 1.000 | 0.040 | 17 | 67902693 | intron variant | G/A | snv | 0.22 | 1 | ||
| rs9480192 | 1.000 | 0.040 | 6 | 150305155 | intergenic variant | C/A;G;T | snv | 1 | |||
| rs259919 | 0.882 | 0.080 | 6 | 30057726 | intron variant | G/A | snv | 0.25 | 6 | ||
| rs1062980 | 0.827 | 0.080 | 15 | 78500185 | 3 prime UTR variant | T/C | snv | 0.39 | 4 | ||
| rs11638372 | 0.925 | 0.080 | 15 | 78691217 | intron variant | C/A;G;T | snv | 0.28 | 3 | ||
| rs12441998 | 0.925 | 0.080 | 15 | 78637030 | intron variant | G/A | snv | 0.63 | 3 | ||
| rs12594247 | 0.925 | 0.080 | 15 | 78654291 | intron variant | C/T | snv | 0.14 | 3 | ||
| rs12910984 | 0.827 | 0.080 | 15 | 78599285 | intron variant | G/A;C;T | snv | 3 | |||
| rs1316971 | 0.925 | 0.080 | 15 | 78638168 | intron variant | A/G;T | snv | 0.62 | 3 | ||
| rs1394371 | 0.925 | 0.080 | 15 | 78432127 | intergenic variant | C/T | snv | 0.22 | 3 | ||
| rs17487514 | 0.925 | 0.080 | 15 | 78661443 | non coding transcript exon variant | C/T | snv | 0.19 | 3 | ||
| rs1903003 | 0.925 | 0.080 | 4 | 88965146 | intron variant | C/G;T | snv | 3 | |||
| rs2036534 | 0.827 | 0.080 | 15 | 78534606 | 3 prime UTR variant | T/C | snv | 0.26 | 3 | ||
| rs2656069 | 0.882 | 0.080 | 15 | 78453365 | intron variant | C/G;T | snv | 3 | |||
| rs3813565 | 0.851 | 0.080 | 15 | 78727268 | splice region variant | G/A;T | snv | 3 | |||
| rs4887053 | 0.925 | 0.080 | 15 | 78420357 | regulatory region variant | A/C;T | snv | 3 | |||
| rs6495309 | 0.807 | 0.080 | 15 | 78622903 | upstream gene variant | C/A;T | snv | 3 | |||
| rs6495314 | 0.925 | 0.080 | 15 | 78668187 | intron variant | A/C | snv | 0.35 | 3 | ||
| rs8038920 | 0.925 | 0.080 | 15 | 78682203 | intron variant | A/G | snv | 0.62 | 3 | ||
| rs938682 | 0.851 | 0.080 | 15 | 78604205 | intron variant | G/A | snv | 0.72 | 3 |