| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs4919510 | 0.641 | 0.520 | 10 | 100975021 | mature miRNA variant | C/G | snv | 0.27 | 0.27 | 32 | |
| rs4150351 | 0.925 | 0.160 | 13 | 102870617 | intron variant | A/C;T | snv | 2 | |||
| rs710100 | 1.000 | 0.040 | 14 | 103135941 | missense variant | A/G | snv | 0.64 | 0.59 | 3 | |
| rs8126 | 0.807 | 0.080 | 14 | 103137232 | 3 prime UTR variant | C/T | snv | 0.63 | 8 | ||
| rs1052823 | 1.000 | 0.040 | 14 | 103137233 | 3 prime UTR variant | G/A;C;T | snv | 0.15 | 3 | ||
| rs1052912 | 1.000 | 0.040 | 14 | 103137316 | 3 prime UTR variant | G/A | snv | 0.13 | 3 | ||
| rs1360602468 | 0.925 | 0.080 | 14 | 103698904 | missense variant | G/C;T | snv | 2 | |||
| rs745564626 | 0.752 | 0.280 | 14 | 103699003 | missense variant | C/G;T | snv | 4.3E-05 | 14 | ||
| rs861539 | 0.519 | 0.680 | 14 | 103699416 | missense variant | G/A | snv | 0.29 | 0.30 | 104 | |
| rs2498804 | 0.827 | 0.160 | 14 | 104766758 | intron variant | C/A;T | snv | 0.40 | 0.33 | 8 | |
| rs121909252 | 1.000 | 0.040 | 13 | 110719667 | missense variant | C/A | snv | 1 | |||
| rs121909250 | 1.000 | 0.040 | 13 | 110719736 | missense variant | G/C | snv | 1 | |||
| rs121909251 | 1.000 | 0.040 | 13 | 110719739 | missense variant | A/G | snv | 1 | |||
| rs2238151 | 1.000 | 0.040 | 12 | 111774029 | intron variant | T/C | snv | 0.52 | 3 | ||
| rs671 | 0.529 | 0.840 | 12 | 111803962 | missense variant | G/A | snv | 1.9E-02 | 5.8E-03 | 116 | |
| rs2012775 | 1.000 | 0.040 | 9 | 115141569 | intron variant | T/C | snv | 0.30 | 2 | ||
| rs776977530 | 0.925 | 0.160 | 5 | 115625723 | synonymous variant | G/A | snv | 4.6E-06 | 2 | ||
| rs26537 | 0.925 | 0.080 | 5 | 115841317 | 3 prime UTR variant | T/C;G | snv | 2 | |||
| rs1057519824 | 0.807 | 0.120 | 7 | 116783374 | missense variant | T/G | snv | 10 | |||
| rs4986790 | 0.438 | 0.800 | 9 | 117713024 | missense variant | A/G;T | snv | 6.1E-02; 4.0E-06 | 223 | ||
| rs4986791 | 0.456 | 0.840 | 9 | 117713324 | missense variant | C/T | snv | 5.7E-02 | 4.9E-02 | 182 | |
| rs397507444 | 0.405 | 0.880 | 1 | 11794407 | missense variant | T/G | snv | 306 | |||
| rs762403278 | 0.851 | 0.200 | 1 | 11796244 | missense variant | T/C;G | snv | 1.6E-05; 4.0E-06 | 4 | ||
| rs1217691063 | 0.330 | 0.920 | 1 | 11796309 | missense variant | A/G | snv | 4.0E-06 | 7.0E-06 | 614 | |
| rs17568 | 0.752 | 0.320 | 1 | 1212042 | synonymous variant | C/T | snv | 0.37 | 0.31 | 12 |