Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs387906666 | 0.827 | 0.080 | 11 | 119278182 | missense variant | A/C;G | snv | 5 | |||
rs74315450 | 0.851 | 0.120 | 21 | 34859485 | missense variant | C/T | snv | 5 | |||
rs780634396 | 0.882 | 0.120 | 18 | 63318618 | missense variant | T/C | snv | 4.0E-06 | 5 | ||
rs869312953 | 0.851 | 0.120 | 1 | 64846735 | missense variant | G/T | snv | 5 | |||
rs10251201 | 0.851 | 0.160 | 7 | 7932654 | intron variant | T/A;C | snv | 4 | |||
rs1188975135 | 0.882 | 0.040 | 22 | 39017772 | missense variant | T/C | snv | 4.0E-06 | 4 | ||
rs121913452 | 0.851 | 0.080 | 9 | 130873027 | missense variant | T/A;C;G | snv | 4 | |||
rs1360698171 | 0.851 | 0.080 | 1 | 182584103 | missense variant | T/C | snv | 4 | |||
rs753000469 | 0.851 | 0.200 | 1 | 212859113 | missense variant | C/T | snv | 4.0E-06 | 4 | ||
rs754944509 | 0.851 | 0.080 | 17 | 42690793 | missense variant | C/T | snv | 4.4E-05 | 4 | ||
rs974120 | 0.851 | 0.200 | 8 | 2789080 | intron variant | T/C;G | snv | 4 | |||
rs2308950 | 0.882 | 0.040 | 1 | 15507011 | missense variant | C/G;T | snv | 4.0E-06; 1.1E-02 | 3 | ||
rs766274360 | 0.882 | 0.040 | 16 | 2713697 | missense variant | G/T | snv | 1.2E-05 | 3 | ||
rs9318227 | 0.882 | 0.080 | 13 | 73926833 | intron variant | T/A;C | snv | 3 | |||
rs10931910 | 0.925 | 0.040 | 2 | 200659013 | intron variant | A/G;T | snv | 2 | |||
rs1258094111 | 0.925 | 0.040 | 14 | 24575388 | missense variant | C/T | snv | 4.0E-06 | 2 | ||
rs201820837 | 0.925 | 0.040 | 12 | 11869532 | missense variant | G/A;T | snv | 2.4E-05; 6.4E-05 | 2 | ||
rs754894156 | 0.925 | 0.040 | 21 | 34834544 | missense variant | C/T | snv | 4.0E-06 | 2 | ||
rs765669662 | 0.925 | 0.040 | 8 | 85465317 | missense variant | G/A;T | snv | 2.0E-05; 4.0E-06 | 2 | ||
rs227092 | 1.000 | 0.040 | 11 | 108366056 | 3 prime UTR variant | G/A;C;T | snv | 1 | |||
rs1408538785 | 0.827 | 0.080 | 6 | 38761760 | missense variant | A/G | snv | 7.0E-06 | 6 | ||
rs762613037 | 0.790 | 0.160 | 21 | 45512196 | missense variant | A/G | snv | 2.1E-05 | 7.0E-06 | 7 | |
rs1482518887 | 0.790 | 0.040 | 21 | 34887018 | missense variant | C/T | snv | 7.0E-06 | 8 | ||
rs1217691063 | 0.330 | 0.920 | 1 | 11796309 | missense variant | A/G | snv | 4.0E-06 | 7.0E-06 | 614 | |
rs387907272 | 0.572 | 0.520 | 3 | 38141150 | stop lost | T/C | snv | 5.2E-05 | 7.0E-06 | 73 |