| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs1217691063 | 0.330 | 0.920 | 1 | 11796309 | missense variant | A/G | snv | 4.0E-06 | 7.0E-06 | 614 | |
| rs1805087 | 0.496 | 0.800 | 1 | 236885200 | missense variant | A/G | snv | 0.20 | 0.21 | 135 | |
| rs1799821 | 0.827 | 0.200 | 1 | 53210776 | missense variant | G/A | snv | 0.49 | 0.46 | 8 | |
| rs2229291 | 0.827 | 0.200 | 1 | 53210729 | missense variant | T/G | snv | 2.3E-02 | 1.5E-02 | 8 | |
| rs368311455 | 0.882 | 0.200 | 1 | 53211185 | missense variant | C/T | snv | 3.2E-05 | 2.8E-05 | 4 | |
| rs1060499537 | 1.000 | 1 | 196429676 | missense variant | A/T | snv | 2 | ||||
| rs751557097 | 1 | 53213431 | missense variant | G/C | snv | 2.8E-05 | 1 | ||||
| rs231775 | 0.504 | 0.720 | 2 | 203867991 | missense variant | A/G;T | snv | 0.42; 4.0E-06 | 115 | ||
| rs281864719 | 0.763 | 0.240 | 2 | 29220831 | missense variant | A/C;G;T | snv | 14 | |||
| rs121918807 | 0.851 | 0.080 | 2 | 165994275 | missense variant | G/A | snv | 7.2E-05 | 2.8E-05 | 5 | |
| rs281864720 | 0.925 | 0.040 | 2 | 29213994 | missense variant | A/C;G;T | snv | 4 | |||
| rs771844443 | 1.000 | 0.040 | 2 | 165309194 | missense variant | A/G | snv | 4.0E-06 | 3 | ||
| rs796053150 | 1.000 | 0.040 | 2 | 165386827 | missense variant | A/G | snv | 3 | |||
| rs114925667 | 0.672 | 0.520 | 3 | 132675903 | missense variant | G/A;T | snv | 1.9E-03; 4.1E-06 | 64 | ||
| rs143319805 | 0.807 | 0.320 | 3 | 193643378 | missense variant | A/G | snv | 6.2E-04 | 5.7E-04 | 12 | |
| rs745386663 | 0.807 | 0.160 | 3 | 33051956 | missense variant | G/A | snv | 8.0E-06 | 2.1E-05 | 7 | |
| rs7041 | 0.576 | 0.800 | 4 | 71752617 | missense variant | A/C;T | snv | 0.52; 4.0E-06 | 64 | ||
| rs222020 | 0.851 | 0.320 | 4 | 71770555 | intron variant | C/T | snv | 0.72 | 5 | ||
| rs1057524792 | 1.000 | 0.040 | 4 | 39467617 | missense variant | T/G | snv | 3 | |||
| rs751866383 | 1.000 | 0.040 | 4 | 39470047 | missense variant | G/T | snv | 4.0E-06 | 3 | ||
| rs866291718 | 1.000 | 0.040 | 4 | 39470042 | missense variant | A/G | snv | 3 | |||
| rs961150638 | 1.000 | 0.040 | 4 | 39470038 | missense variant | G/C | snv | 4.0E-06 | 3 | ||
| rs397514611 | 1.000 | 6 | 5545261 | missense variant | T/C | snv | 1.2E-05 | 2 | |||
| rs397514612 | 1.000 | 6 | 5613275 | missense variant | A/T | snv | 1.6E-05 | 7.0E-06 | 2 | ||
| rs1554616628 | 1.000 | 7 | 76329927 | missense variant | G/A | snv | 2 |