| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs143319805 | 0.807 | 0.320 | 3 | 193643378 | missense variant | A/G | snv | 6.2E-04 | 5.7E-04 | 12 | |
| rs80356529 | 0.827 | 0.240 | 3 | 193643996 | missense variant | G/A;C | snv | 9 | |||
| rs11258194 | 0.776 | 0.160 | 10 | 13110400 | missense variant | T/A | snv | 4.4E-02 | 6.0E-02 | 9 | |
| rs387906930 | 0.790 | 0.360 | 4 | 6301846 | missense variant | C/G;T | snv | 8 | |||
| rs74315205 | 0.807 | 0.360 | 4 | 6302385 | missense variant | G/A | snv | 7 | |||
| rs80356530 | 0.882 | 0.320 | 3 | 193667168 | splice region variant | TTAG/- | delins | 4 | |||
| rs398124298 | 0.925 | 0.160 | 3 | 193647110 | missense variant | C/A;G | snv | 3 | |||
| rs765208285 | 0.925 | 0.160 | 3 | 193662945 | missense variant | G/A | snv | 1.6E-05 | 3 | ||
| rs10451941 | 0.882 | 0.160 | 3 | 193637313 | intron variant | T/A;C | snv | 0.42 | 3 | ||
| rs121908375 | 0.882 | 0.160 | 3 | 193637280 | missense variant | G/A | snv | 3 | |||
| rs151103940 | 0.882 | 0.160 | 3 | 193614929 | missense variant | A/G | snv | 4.0E-04 | 1.1E-03 | 3 | |
| rs9838374 | 0.882 | 0.240 | 3 | 193598916 | intron variant | C/T | snv | 0.22 | 3 | ||
| rs80356525 | 0.882 | 0.200 | 19 | 45553741 | stop gained | G/A;C | snv | 3 | |||
| rs414237 | 0.925 | 0.200 | 3 | 193668749 | 3 prime UTR variant | C/G;T | snv | 0.71 | 2 | ||
| rs879255592 | 0.925 | 0.160 | 3 | 193647127 | missense variant | G/A | snv | 2 | |||
| rs145413511 | 0.925 | 0.160 | 1 | 12007062 | missense variant | G/A | snv | 4.0E-06 | 7.0E-06 | 2 | |
| rs1374279494 | 0.925 | 0.160 | 3 | 193635422 | missense variant | A/T | snv | 4.0E-06 | 2 | ||
| rs166850 | 0.925 | 0.160 | 3 | 193637285 | splice region variant | T/A;C | snv | 0.87 | 2 | ||
| rs190223702 | 0.925 | 0.160 | 3 | 193642978 | missense variant | G/A | snv | 2.8E-05 | 1.4E-05 | 2 | |
| rs28939082 | 0.925 | 0.160 | 3 | 193637980 | missense variant | G/A | snv | 2 | |||
| rs387906900 | 0.925 | 0.160 | 3 | 193643978 | missense variant | G/T | snv | 2 | |||
| rs398124303 | 0.925 | 0.160 | 3 | 193638064 | missense variant | A/C;G | snv | 4.0E-06 | 2 | ||
| rs765118029 | 0.925 | 0.160 | 3 | 193635443 | missense variant | G/A | snv | 2.0E-05 | 5.6E-05 | 2 | |
| rs770966290 | 0.925 | 0.160 | 3 | 193638010 | missense variant | A/G | snv | 1.6E-05 | 4.2E-05 | 2 | |
| rs780333963 | 1.000 | 0.160 | 3 | 193637279 | missense variant | C/T | snv | 8.0E-06 | 2 |