| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs4727443 | 7 | 99995723 | upstream gene variant | C/A;G | snv | 1 | |||||
| rs6974373 | 7 | 99993270 | upstream gene variant | C/A;G | snv | 1 | |||||
| rs13542 | 1.000 | 0.080 | 13 | 99986138 | 3 prime UTR variant | G/A | snv | 0.30 | 1 | ||
| rs7696536 | 0.925 | 0.120 | 4 | 9998612 | intron variant | G/T | snv | 0.24 | 3 | ||
| rs2525556 | 7 | 99980121 | upstream gene variant | T/C | snv | 0.35 | 1 | ||||
| rs2283017 | 7 | 99977135 | intron variant | A/G | snv | 0.35 | 1 | ||||
| rs10008035 | 0.925 | 0.120 | 4 | 9997711 | intron variant | G/A;T | snv | 3 | |||
| rs13113918 | 0.925 | 0.120 | 4 | 9996869 | synonymous variant | A/G | snv | 0.80 | 0.79 | 3 | |
| rs10939650 | 0.925 | 0.120 | 4 | 9996816 | synonymous variant | C/G;T | snv | 1.2E-05; 0.70 | 3 | ||
| rs16891971 | 0.925 | 0.120 | 4 | 9996752 | intron variant | C/A;T | snv | 2.7E-02; 4.0E-06 | 2 | ||
| rs7669607 | 0.925 | 0.120 | 4 | 9996177 | intron variant | T/C | snv | 0.80 | 3 | ||
| rs10760706 | 1.000 | 0.040 | 9 | 99961410 | intron variant | C/T | snv | 0.69 | 1 | ||
| rs3733587 | 0.925 | 0.120 | 4 | 9995810 | non coding transcript exon variant | A/G | snv | 0.24 | 3 | ||
| rs3733588 | 0.925 | 0.120 | 4 | 9995679 | non coding transcript exon variant | G/A | snv | 0.72 | 3 | ||
| rs4529048 | 0.925 | 0.120 | 4 | 9995488 | intron variant | C/A;T | snv | 3 | |||
| rs4547795 | 0.925 | 0.120 | 4 | 9995436 | intron variant | C/T | snv | 0.24 | 3 | ||
| rs13111638 | 0.882 | 0.200 | 4 | 9995266 | intron variant | T/C | snv | 0.82 | 3 | ||
| rs2581360 | 15 | 99951677 | regulatory region variant | C/T | snv | 0.28 | 1 | ||||
| rs9998739 | 0.925 | 0.120 | 4 | 9994885 | intron variant | G/A | snv | 0.23 | 3 | ||
| rs3796842 | 0.925 | 0.120 | 4 | 9994227 | intron variant | A/T | snv | 0.48 | 3 | ||
| rs12499857 | 0.925 | 0.120 | 4 | 9993752 | intron variant | G/A | snv | 0.45 | 3 | ||
| rs10256972 | 7 | 999367 | intron variant | A/C | snv | 0.62 | 1 | ||||
| rs2573674 | 15 | 99936478 | intergenic variant | C/A | snv | 0.28 | 1 | ||||
| rs3775948 | 0.882 | 0.160 | 4 | 9993558 | intron variant | G/A;C | snv | 3 | |||
| rs6449213 | 0.827 | 0.240 | 4 | 9992591 | intron variant | C/T | snv | 0.82 | 3 |