| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs8192284 | 0.724 | 0.720 | 1 | 154454494 | missense variant | A/C;T | snv | 19 | |||
| rs3811463 | 0.752 | 0.400 | 1 | 26427451 | 3 prime UTR variant | T/A;C | snv | 14 | |||
| rs5744174 | 0.742 | 0.360 | 1 | 223111186 | missense variant | A/G | snv | 0.39 | 0.34 | 13 | |
| rs12733285 | 0.776 | 0.120 | 1 | 202952912 | intron variant | C/T | snv | 0.26 | 12 | ||
| rs1342387 | 0.776 | 0.120 | 1 | 202945228 | intron variant | T/C | snv | 0.53 | 12 | ||
| rs6682925 | 0.776 | 0.160 | 1 | 67165579 | intron variant | C/T | snv | 0.47 | 11 | ||
| rs1380576 | 0.763 | 0.240 | 1 | 204519150 | intron variant | G/C | snv | 0.57 | 10 | ||
| rs5277 | 0.790 | 0.160 | 1 | 186679065 | synonymous variant | C/G;T | snv | 0.12; 8.0E-06 | 9 | ||
| rs689470 | 0.776 | 0.240 | 1 | 186671926 | 3 prime UTR variant | G/A;C;T | snv | 9 | |||
| rs3790843 | 0.827 | 0.160 | 1 | 200041696 | intron variant | C/T | snv | 0.29 | 7 | ||
| rs5273 | 0.827 | 0.080 | 1 | 186674636 | missense variant | A/C;G | snv | 4.0E-06; 7.6E-03 | 1.4E-02 | 6 | |
| rs6672420 | 0.827 | 0.120 | 1 | 24964519 | missense variant | A/T | snv | 0.56 | 0.50 | 6 | |
| rs12904 | 0.827 | 0.160 | 1 | 155134221 | 3 prime UTR variant | G/A | snv | 0.40 | 5 | ||
| rs2070803 | 0.925 | 0.080 | 1 | 155185239 | intron variant | G/A | snv | 0.55 | 5 | ||
| rs2990245 | 0.827 | 0.240 | 1 | 155227671 | upstream gene variant | C/G;T | snv | 5 | |||
| rs6128 | 0.851 | 0.360 | 1 | 169593666 | synonymous variant | C/A;T | snv | 2.8E-05; 0.24 | 5 | ||
| rs621559 | 0.827 | 0.080 | 1 | 43179740 | intron variant | G/A | snv | 0.18 | 5 | ||
| rs753535070 | 0.851 | 0.120 | 1 | 155187350 | missense variant | T/C | snv | 8.0E-06 | 5 | ||
| rs10746463 | 0.851 | 0.200 | 1 | 207337251 | missense variant | G/A;T | snv | 4 | |||
| rs111238176 | 0.851 | 0.160 | 1 | 172665840 | missense variant | A/G | snv | 4 | |||
| rs1200055659 | 0.851 | 0.080 | 1 | 153614902 | missense variant | G/A | snv | 7.0E-06 | 4 | ||
| rs4460629 | 0.882 | 0.080 | 1 | 155162859 | intergenic variant | T/C | snv | 0.56 | 4 | ||
| rs9426886 | 0.851 | 0.200 | 1 | 155179278 | intron variant | A/T | snv | 0.40 | 4 | ||
| rs1064261 | 0.925 | 0.080 | 1 | 11228701 | missense variant | G/A;T | snv | 0.75; 4.0E-06 | 3 | ||
| rs114673809 | 0.882 | 0.080 | 1 | 11787703 | 3 prime UTR variant | G/A | snv | 5.0E-03 | 3 |