| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs1051849 | 1.000 | 0.040 | 17 | 37513222 | 3 prime UTR variant | T/C | snv | 9.9E-02 | 1 | ||
| rs1057519702 | 1.000 | 0.040 | 4 | 54726020 | missense variant | T/C | snv | 1 | |||
| rs1057519731 | 0.925 | 0.040 | 15 | 66436816 | missense variant | G/C | snv | 1 | |||
| rs1057519804 | 1.000 | 0.040 | 14 | 104776711 | missense variant | G/T | snv | 1 | |||
| rs1057519807 | 1.000 | 0.040 | 19 | 4110586 | missense variant | A/T | snv | 1 | |||
| rs1057519837 | 1.000 | 0.040 | 3 | 41224631 | missense variant | C/G;T | snv | 1 | |||
| rs1057519856 | 0.925 | 0.040 | 15 | 66436815 | missense variant | T/A | snv | 1 | |||
| rs1057520031 | 1.000 | 0.040 | 4 | 54727440 | missense variant | A/C;G | snv | 1 | |||
| rs1060502550 | 1.000 | 0.040 | 4 | 54727488 | missense variant | A/G | snv | 1 | |||
| rs1063045 | 1.000 | 0.040 | 8 | 89982791 | synonymous variant | C/T | snv | 0.35 | 0.33 | 1 | |
| rs1110400 | 1.000 | 0.040 | 16 | 89919722 | missense variant | T/C | snv | 5.6E-03 | 6.6E-03 | 1 | |
| rs11547464 | 1.000 | 0.040 | 16 | 89919683 | missense variant | G/A | snv | 5.3E-03 | 4.7E-03 | 1 | |
| rs11551405 | 1.000 | 0.040 | 3 | 53284850 | 3 prime UTR variant | C/A | snv | 0.16 | 1 | ||
| rs11552823 | 1.000 | 0.040 | 9 | 21971117 | missense variant | G/A;C | snv | 4.3E-06 | 1 | ||
| rs1156242341 | 1.000 | 0.040 | 2 | 222202072 | missense variant | T/C | snv | 7.0E-06 | 1 | ||
| rs11568953 | 1.000 | 0.040 | 4 | 109963240 | synonymous variant | A/G | snv | 9.7E-03 | 1.0E-02 | 1 | |
| rs1176796243 | 1.000 | 0.040 | 3 | 69941240 | missense variant | A/G | snv | 1 | |||
| rs1194330242 | 1.000 | 0.040 | 16 | 4681743 | missense variant | A/G | snv | 1.4E-05 | 1 | ||
| rs121909233 | 1.000 | 0.040 | 10 | 87864524 | missense variant | G/A | snv | 1 | |||
| rs121913248 | 1.000 | 0.040 | 1 | 114716109 | missense variant | C/G;T | snv | 4.0E-06 | 1 | ||
| rs121913523 | 1.000 | 0.040 | 4 | 54728092 | missense variant | T/A;C | snv | 1 | |||
| rs1231071385 | 1.000 | 0.040 | 2 | 175093177 | frameshift variant | -/G | ins | 1 | |||
| rs1264171723 | 1.000 | 0.040 | 20 | 57266050 | missense variant | G/A | snv | 7.0E-06 | 1 | ||
| rs1269304342 | 1.000 | 0.040 | 10 | 98425560 | missense variant | C/T | snv | 7.0E-06 | 1 | ||
| rs1278609613 | 1.000 | 0.040 | 4 | 147542604 | missense variant | G/A;C;T | snv | 4.0E-06; 4.0E-06; 8.0E-06 | 1 |