| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs543719221 | 3 | 8105663 | intron variant | G/A;T | snv | 1 | |||||
| rs9847133 | 1.000 | 0.080 | 3 | 8208835 | intron variant | C/T | snv | 0.54 | 1 | ||
| rs388458 | 3 | 8186943 | intron variant | C/G;T | snv | 1 | |||||
| rs9816551 | 1.000 | 0.040 | 3 | 8292844 | intron variant | C/G | snv | 0.48 | 1 | ||
| rs13317787 | 3 | 8100265 | intron variant | C/A | snv | 6.7E-02 | 1 | ||||
| rs359027 | 3 | 8403337 | intron variant | A/G | snv | 0.77 | 1 | ||||
| rs10510388 | 3 | 8215887 | intron variant | A/C | snv | 0.28 | 1 | ||||
| rs17048879 | 3 | 8233854 | intron variant | T/C | snv | 0.31 | 1 | ||||
| rs6777332 | 3 | 8182251 | intron variant | C/G;T | snv | 1 | |||||
| rs1554194 | 3 | 8096354 | intron variant | G/C | snv | 0.48 | 1 | ||||
| rs9862842 | 3 | 8101617 | intron variant | T/C | snv | 0.39 | 1 | ||||
| rs1994876 | 3 | 8507979 | intron variant | C/T | snv | 0.53 | 1 | ||||
| rs4686203 | 1.000 | 0.040 | 3 | 7954649 | non coding transcript exon variant | G/A;T | snv | 1 | |||
| rs9846963 | 1.000 | 0.040 | 3 | 7955165 | intron variant | C/T | snv | 0.37 | 1 | ||
| rs9872473 | 1.000 | 0.040 | 3 | 7952986 | non coding transcript exon variant | G/A | snv | 0.35 | 1 | ||
| rs1485149 | 1.000 | 0.040 | 3 | 7971765 | intron variant | A/C;G | snv | 1 | |||
| rs35144233 | 1.000 | 0.080 | 3 | 8012910 | intron variant | G/A | snv | 2.3E-02 | 1 | ||
| rs171408 | 1.000 | 0.040 | 3 | 8567234 | intron variant | G/A;T | snv | 1 | |||
| rs4349489 | 3 | 8501609 | non coding transcript exon variant | G/C | snv | 0.53 | 1 | ||||
| rs1157280 | 1.000 | 0.040 | 3 | 7967341 | intron variant | G/T | snv | 0.16 | 1 | ||
| rs7624284 | 1.000 | 0.040 | 3 | 7954250 | non coding transcript exon variant | T/C | snv | 8.5E-02 | 1 | ||
| rs7624374 | 1.000 | 0.040 | 3 | 7954315 | non coding transcript exon variant | T/C | snv | 8.1E-02 | 1 | ||
| rs4686205 | 1.000 | 0.040 | 3 | 7967006 | intron variant | T/C | snv | 0.28 | 1 | ||
| rs7643459 | 0.925 | 0.120 | 3 | 7963141 | intron variant | G/C;T | snv | 1 |