Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs587777186 | 0.925 | 18 | 62146023 | missense variant | A/G;T | snv | 3 | ||||
rs869025322 | 0.925 | 0.040 | 4 | 88521653 | missense variant | A/G | snv | 3 | |||
rs1206736425 | 1 | 161626229 | missense variant | T/C | snv | 2 | |||||
rs137854438 | 1.000 | 0.080 | 8 | 143728570 | stop gained | A/T | snv | 2 | |||
rs1387329667 | 9 | 136500595 | missense variant | G/A | snv | 2 | |||||
rs387906617 | 2 | 207567506 | missense variant | A/G | snv | 2 | |||||
rs504849 | 3 | 55488911 | intron variant | T/C;G | snv | 1 | |||||
rs524153 | 3 | 55491957 | upstream gene variant | T/A;G | snv | 1 | |||||
rs1217691063 | 0.330 | 0.920 | 1 | 11796309 | missense variant | A/G | snv | 4.0E-06 | 7.0E-06 | 614 | |
rs757956956 | 19 | 34377533 | missense variant | A/G | snv | 4.0E-06 | 1 | ||||
rs121918214 | 1.000 | 0.200 | 16 | 53873837 | missense variant | G/A | snv | 4.0E-06 | 7.0E-06 | 3 | |
rs781028867 | 1.000 | 0.200 | 16 | 53873846 | missense variant | C/A;T | snv | 4.0E-06 | 3 | ||
rs201405525 | 0.925 | 0.240 | 8 | 90044993 | missense variant | G/A;C | snv | 4.5E-04; 4.0E-06 | 3 | ||
rs1234344050 | 2 | 188984825 | missense variant | C/G | snv | 4.0E-06 | 2 | ||||
rs28939086 | 0.925 | 0.160 | 7 | 107690220 | missense variant | A/C;G | snv | 2.0E-04; 4.0E-06 | 4 | ||
rs368705607 | 0.882 | 0.120 | 1 | 226225766 | missense variant | T/C;G | snv | 2.8E-05; 4.0E-06 | 7 | ||
rs1052108705 | 6 | 31165217 | missense variant | C/T | snv | 4.1E-06 | 2.1E-05 | 3 | |||
rs121918355 | 0.807 | 0.280 | 14 | 74555629 | stop gained | G/A;T | snv | 2.1E-05; 4.2E-06 | 7 | ||
rs121913483 | 0.649 | 0.560 | 4 | 1801841 | missense variant | C/A;G;T | snv | 4.2E-06; 1.3E-05 | 31 | ||
rs746147592 | 1.000 | 0.160 | X | 100665627 | missense variant | G/A;C | snv | 5.5E-06 | 2 | ||
rs80338852 | 0.925 | 0.200 | 13 | 31317599 | stop gained | T/A;C | snv | 8.0E-06 | 3 | ||
rs104893951 | 0.851 | 0.080 | 6 | 1610780 | missense variant | T/A;C | snv | 8.0E-06 | 5 | ||
rs764120087 | 22 | 41117439 | missense variant | G/A | snv | 8.0E-06 | 2 | ||||
rs768746587 | 6 | 31165136 | missense variant | C/T | snv | 8.4E-06 | 3 | ||||
rs775144154 | 0.627 | 0.600 | 21 | 45531904 | missense variant | C/A;T | snv | 9.7E-06; 1.4E-05 | 38 |