| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs764255410 | 1.000 | 0.080 | 2 | 147918546 | missense variant | G/A | snv | 1 | |||
| rs1057519896 | 0.742 | 0.320 | 4 | 152326136 | missense variant | C/A;T | snv | 12 | |||
| rs149680468 | 0.742 | 0.320 | 4 | 152326137 | missense variant | G/A;C;T | snv | 12 | |||
| rs866987936 | 0.752 | 0.240 | 4 | 152326214 | missense variant | C/A;G;T | snv | 12 | |||
| rs747241612 | 0.752 | 0.240 | 4 | 152326215 | missense variant | G/C | snv | 4.0E-06 | 12 | ||
| rs1057519895 | 0.724 | 0.240 | 4 | 152328232 | missense variant | C/A;G;T | snv | 15 | |||
| rs867384286 | 0.732 | 0.240 | 4 | 152328233 | missense variant | G/A;C | snv | 4.3E-06 | 14 | ||
| rs140081212 | 0.925 | 0.080 | 1 | 155215184 | non coding transcript exon variant | G/A | snv | 2 | |||
| rs779372373 | 1.000 | 0.080 | 5 | 157244381 | missense variant | G/A | snv | 1.2E-05 | 7.0E-06 | 1 | |
| rs1057519875 | 0.925 | 0.120 | 2 | 157770385 | missense variant | C/A | snv | 2 | |||
| rs863224846 | 0.882 | 0.160 | 2 | 157770386 | missense variant | T/C;G | snv | 4.0E-06 | 3 | ||
| rs922655349 | 1.000 | 0.080 | 1 | 16131867 | missense variant | C/T | snv | 1 | |||
| rs141014084 | 1.000 | 0.080 | 5 | 177430911 | missense variant | G/A | snv | 2.0E-05 | 2.1E-05 | 1 | |
| rs1003158162 | 1.000 | 0.080 | 2 | 178531968 | missense variant | G/A | snv | 4.0E-06 | 1 | ||
| rs756924372 | 1.000 | 0.080 | 2 | 178534461 | missense variant | G/A;C | snv | 4.0E-06 | 1 | ||
| rs397517769 | 1.000 | 0.080 | 2 | 178542408 | missense variant | C/T | snv | 5.6E-05 | 1.4E-05 | 1 | |
| rs55713867 | 1.000 | 0.080 | 2 | 178575658 | missense variant | A/G | snv | 1 | |||
| rs373526624 | 1.000 | 0.080 | 2 | 178607095 | missense variant | C/T | snv | 7.0E-04 | 1.6E-04 | 1 | |
| rs199684560 | 1.000 | 0.080 | 2 | 178633512 | missense variant | G/A | snv | 7.3E-05 | 4.2E-05 | 1 | |
| rs539470256 | 1.000 | 0.080 | 2 | 178779033 | missense variant | C/T | snv | 1.3E-04 | 7.7E-05 | 1 | |
| rs749415085 | 0.807 | 0.160 | 3 | 179198937 | missense variant | C/A;G;T | snv | 7 | |||
| rs772110575 | 0.807 | 0.160 | 3 | 179198938 | missense variant | G/A;T | snv | 4.0E-06 | 7 | ||
| rs121913287 | 0.752 | 0.400 | 3 | 179199088 | missense variant | G/A | snv | 12 | |||
| rs1057519933 | 0.790 | 0.240 | 3 | 179199156 | missense variant | A/G | snv | 11 | |||
| rs1057519935 | 0.790 | 0.240 | 3 | 179199157 | missense variant | A/G | snv | 11 |