| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs199473063 | 1.000 | 0.080 | 3 | 38620929 | missense variant | C/G | snv | 1 | |||
| rs199473065 | 1.000 | 0.080 | 3 | 38620921 | missense variant | G/C | snv | 1 | |||
| rs199473066 | 1.000 | 0.080 | 3 | 38620910 | missense variant | A/G | snv | 1 | |||
| rs199473067 | 1.000 | 0.080 | 3 | 38620900 | missense variant | G/A;T | snv | 1.6E-05 | 1 | ||
| rs199473558 | 1.000 | 0.080 | 3 | 38620894 | missense variant | G/A;C | snv | 1.6E-05 | 1 | ||
| rs199473559 | 1.000 | 0.080 | 3 | 38620843 | missense variant | G/A;T | snv | 1 | |||
| rs199473070 | 0.925 | 0.120 | 3 | 38613811 | missense variant | A/G;T | snv | 2 | |||
| rs45620037 | 0.882 | 0.120 | 3 | 38613787 | missense variant | G/A | snv | 6.6E-04 | 6.6E-04 | 2 | |
| rs45546039 | 0.732 | 0.120 | 3 | 38613781 | missense variant | C/A;T | snv | 4.1E-06 | 2 | ||
| rs199473560 | 1.000 | 0.080 | 3 | 38613779 | missense variant | C/G | snv | 1 | |||
| rs199473072 | 0.827 | 0.160 | 3 | 38613773 | missense variant | G/A | snv | 1.2E-05 | 8.4E-05 | 3 | |
| rs199473071 | 0.925 | 0.120 | 3 | 38613772 | missense variant | C/T | snv | 1.7E-05 | 1.4E-05 | 1 | |
| rs199473561 | 0.882 | 0.120 | 3 | 38613769 | missense variant | G/A | snv | 9.1E-05 | 3.5E-05 | 1 | |
| rs199473074 | 1.000 | 0.080 | 3 | 38613758 | missense variant | T/C | snv | 4.2E-06 | 1 | ||
| rs45471994 | 0.925 | 0.080 | 3 | 38613752 | missense variant | C/T | snv | 1.1E-04 | 4.0E-04 | 1 | |
| rs199473076 | 0.925 | 0.120 | 3 | 38609950 | missense variant | C/T | snv | 8.0E-06 | 2.8E-05 | 2 | |
| 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 | |
| rs199473079 | 1.000 | 0.080 | 3 | 38609860 | missense variant | G/T | snv | 1 | |||
| rs199473080 | 1.000 | 0.120 | 3 | 38609843 | missense variant | G/T | snv | 1 | |||
| rs199473081 | 1.000 | 0.080 | 3 | 38609841 | missense variant | A/T | snv | 1 | |||
| rs199473562 | 1.000 | 0.080 | 3 | 38609836 | missense variant | G/C | snv | 1 | |||
| rs199473082 | 1.000 | 0.080 | 3 | 38609824 | missense variant | G/A;C | snv | 1 | |||
| rs199473083 | 0.925 | 0.080 | 3 | 38609823 | missense variant | C/T | snv | 1.6E-05 | 1 | ||
| rs199473084 | 1.000 | 0.120 | 3 | 38609803 | missense variant | C/G;T | snv | 1.6E-05 | 1 |