| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs137854605 | 1.000 | 0.120 | 3 | 38581337 | missense variant | GA/TT | mnv | 1 | |||
| rs137854610 | 0.925 | 0.120 | 3 | 38550895 | missense variant | C/T | snv | 2.8E-05 | 1.7E-04 | 1 | |
| rs137854614 | 0.882 | 0.120 | 3 | 38550988 | missense variant | T/C | snv | 1 | |||
| rs137854615 | 0.851 | 0.120 | 3 | 38550989 | missense variant | A/G | snv | 1 | |||
| rs137854619 | 0.925 | 0.120 | 3 | 38550917 | missense variant | C/T | snv | 2.7E-04 | 7.7E-05 | 1 | |
| rs150264233 | 1.000 | 0.120 | 3 | 38550661 | stop gained | G/A;T | snv | 1.3E-04 | 3.9E-04 | 1 | |
| rs184442491 | 1.000 | 0.120 | 3 | 38603888 | missense variant | C/A | snv | 2.1E-04 | 7.7E-04 | 1 | |
| rs185638763 | 0.882 | 0.120 | 3 | 38599001 | missense variant | G/A;T | snv | 1.2E-05 | 1 | ||
| rs199473043 | 1.000 | 0.120 | 3 | 38633282 | missense variant | C/A | snv | 1 | |||
| rs199473047 | 1.000 | 0.120 | 3 | 38633180 | missense variant | C/G;T | snv | 4.8E-05 | 1 | ||
| rs199473048 | 1.000 | 0.120 | 3 | 38633166 | missense variant | C/T | snv | 5.3E-05 | 5.6E-05 | 1 | |
| rs199473049 | 1.000 | 0.120 | 3 | 38633150 | missense variant | C/T | snv | 1.2E-05 | 2.1E-05 | 1 | |
| rs199473057 | 1.000 | 0.120 | 3 | 38630360 | missense variant | T/C | snv | 1 | |||
| rs199473059 | 1.000 | 0.120 | 3 | 38630330 | missense variant | C/G;T | snv | 2.2E-04 | 1 | ||
| rs199473071 | 0.925 | 0.120 | 3 | 38613772 | missense variant | C/T | snv | 1.7E-05 | 1.4E-05 | 1 | |
| rs199473077 | 1.000 | 0.120 | 3 | 38609935 | missense variant | G/T | snv | 8.0E-06 | 7.0E-06 | 1 | |
| rs199473078 | 1.000 | 0.120 | 3 | 38609929 | missense variant | C/G | snv | 5.6E-05 | 4.2E-05 | 1 | |
| rs199473080 | 1.000 | 0.120 | 3 | 38609843 | missense variant | G/T | snv | 1 | |||
| rs199473084 | 1.000 | 0.120 | 3 | 38609803 | missense variant | C/G;T | snv | 1.6E-05 | 1 | ||
| rs199473094 | 1.000 | 0.120 | 3 | 38606791 | missense variant | G/A | snv | 4.0E-06 | 7.0E-06 | 1 | |
| rs199473099 | 1.000 | 0.120 | 3 | 38606700 | missense variant | G/A | snv | 1 | |||
| rs199473105 | 1.000 | 0.120 | 3 | 38606099 | missense variant | A/G | snv | 7.0E-06 | 1 | ||
| rs199473107 | 1.000 | 0.120 | 3 | 38606078 | missense variant | A/T | snv | 1 | |||
| rs199473108 | 0.925 | 0.120 | 3 | 38606071 | missense variant | G/A;C;T | snv | 1.2E-05 | 1 | ||
| rs199473109 | 1.000 | 0.120 | 3 | 38606064 | missense variant | G/C | snv | 1 |