| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs763351020 | 0.633 | 0.560 | 7 | 101132046 | missense variant | C/T | snv | 4.0E-06 | 35 | ||
| rs1799889 | 0.649 | 0.600 | 7 | 101126430 | upstream gene variant | A/G | snv | 31 | |||
| rs2227631 | 0.742 | 0.200 | 7 | 101126257 | upstream gene variant | A/G | snv | 0.54 | 13 | ||
| rs1799768 | 0.807 | 0.360 | 7 | 101126425 | upstream gene variant | -/A;C | ins | 6 | |||
| rs6092 | 0.807 | 0.200 | 7 | 101128436 | missense variant | G/A | snv | 9.5E-02 | 8.0E-02 | 6 | |
| rs1411224107 | 0.882 | 0.160 | 7 | 101128439 | missense variant | C/T | snv | 7.0E-06 | 4 | ||
| rs769665945 | 0.882 | 0.160 | 7 | 101137079 | missense variant | C/A;T | snv | 4.0E-06; 3.6E-05 | 3 | ||
| rs1400537035 | 0.882 | 0.200 | 7 | 101131931 | missense variant | C/A;G;T | snv | 3 | |||
| rs773829498 | 0.882 | 0.080 | 7 | 101130457 | missense variant | A/G | snv | 4.0E-06 | 3 | ||
| rs532966772 | 1.000 | 0.080 | 7 | 101132023 | synonymous variant | C/T | snv | 4.0E-06 | 1 | ||
| rs2070682 | 1.000 | 0.120 | 7 | 101133986 | intron variant | T/C | snv | 0.44 | 1 | ||
| rs1402686368 | 1.000 | 0.040 | 7 | 101133793 | missense variant | G/A | snv | 4.0E-06 | 7.0E-06 | 1 | |
| rs6090 | 1.000 | 0.040 | 7 | 101128442 | missense variant | G/A | snv | 2.9E-02 | 3.3E-02 | 1 | |
| rs7242 | 1.000 | 0.040 | 7 | 101138164 | 3 prime UTR variant | T/G | snv | 0.44 | 1 | ||
| rs2227684 | 1.000 | 0.040 | 7 | 101133650 | intron variant | G/A;T | snv | 0.41 | 1 | ||
| rs1442033697 | 7 | 101135780 | frameshift variant | A/- | del | 1 | |||||
| rs1349041080 | 1.000 | 0.080 | 7 | 101137084 | splice donor variant | G/- | delins | 4.0E-06 | 1 | ||
| rs1435953393 | 1.000 | 0.080 | 7 | 101137405 | missense variant | G/A | snv | 1.6E-05 | 1.4E-05 | 1 |