Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs745382803 | 1.000 | 0.040 | 3 | 69965076 | missense variant | C/A;G | snv | 4.0E-06; 4.0E-06 | 1 | ||
rs907102077 | 1.000 | 0.040 | 3 | 9760752 | missense variant | G/A | snv | 1 | |||
rs1484691555 | 1.000 | 0.040 | 20 | 9539512 | missense variant | C/T | snv | 4.0E-06 | 1 | ||
rs1277219458 | 1.000 | 0.040 | 2 | 241143002 | missense variant | C/T | snv | 1 | |||
rs779173667 | 1.000 | 0.040 | 4 | 54290418 | missense variant | G/A | snv | 8.0E-06 | 1.4E-05 | 1 | |
rs267605306 | 1.000 | 0.040 | 19 | 14446504 | missense variant | C/G;T | snv | 1.6E-05 | 1 | ||
rs55735910 | 1.000 | 0.040 | 8 | 47881444 | missense variant | G/A | snv | 1.4E-05 | 1 | ||
rs267600891 | 1.000 | 0.040 | 6 | 166469882 | missense variant | C/T | snv | 1 | |||
rs755753950 | 1.000 | 0.040 | 22 | 40405688 | missense variant | G/A | snv | 4.4E-05 | 2.1E-05 | 1 | |
rs564777385 | 1.000 | 0.040 | 2 | 178800635 | missense variant | C/G;T | snv | 3.6E-05 | 1 | ||
rs267599092 | 1.000 | 0.040 | 2 | 178779043 | missense variant | C/T | snv | 1 | |||
rs1204056923 | 1.000 | 0.040 | 2 | 178590160 | missense variant | C/T | snv | 1.4E-05 | 1 | ||
rs369098292 | 1.000 | 0.040 | 2 | 178572742 | missense variant | G/A | snv | 4.0E-06 | 1.4E-05 | 1 | |
rs374713701 | 1.000 | 0.040 | 2 | 178593660 | missense variant | C/A;T | snv | 4.0E-06; 8.1E-06 | 1 | ||
rs1458591077 | 1.000 | 0.040 | 2 | 178630352 | missense variant | C/T | snv | 1 | |||
rs375422359 | 1.000 | 0.040 | 2 | 178563634 | missense variant | C/T | snv | 2.4E-05 | 3.5E-05 | 1 | |
rs764005465 | 1.000 | 0.040 | 2 | 178572808 | missense variant | C/T | snv | 8.1E-06 | 1 |