Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs1337040042 | 1.000 | 0.040 | 17 | 81131085 | start lost | T/C | snv | 1 | |||
rs773301216 | 1.000 | 0.040 | 7 | 91118066 | missense variant | G/A | snv | 4.0E-06 | 1.4E-05 | 1 | |
rs755711267 | 1.000 | 0.040 | 4 | 75607279 | missense variant | C/T | snv | 3.6E-05 | 2.8E-05 | 1 | |
rs1057519893 | 0.790 | 0.160 | 12 | 56085070 | missense variant | G/A;T | snv | 1 | |||
rs753734841 | 1.000 | 0.040 | 2 | 27440906 | missense variant | C/T | snv | 1.2E-05 | 1.4E-05 | 1 | |
rs375029799 | 1.000 | 0.040 | 2 | 178776873 | missense variant | C/T | snv | 2.4E-05 | 2.1E-05 | 1 | |
rs200212150 | 1.000 | 0.040 | 12 | 40314084 | missense variant | G/A;T | snv | 1.6E-05 | 1.4E-05 | 1 | |
rs144052967 | 1.000 | 0.040 | 9 | 36665552 | missense variant | C/T | snv | 1.3E-04 | 6.3E-05 | 1 | |
rs1423134583 | 1.000 | 0.040 | 10 | 26096393 | missense variant | T/A | snv | 4.0E-06 | 1 | ||
rs201821707 | 1.000 | 0.040 | 3 | 27346152 | missense variant | G/A;C;T | snv | 3.4E-04; 6.0E-05; 4.0E-06 | 1 | ||
rs374535834 | 1.000 | 0.040 | 11 | 67435048 | missense variant | C/A;T | snv | 4.1E-06; 6.5E-05 | 1 | ||
rs746238409 | 1.000 | 0.040 | 3 | 134202791 | missense variant | C/T | snv | 2.8E-05 | 2.1E-05 | 1 | |
rs368877591 | 1.000 | 0.040 | 3 | 43348090 | missense variant | G/A | snv | 5.9E-05 | 1.4E-05 | 1 | |
rs762000831 | 1.000 | 0.040 | 2 | 219483170 | missense variant | C/T | snv | 8.9E-05 | 1.4E-05 | 1 | |
rs113498671 | 1.000 | 0.040 | 3 | 195884972 | missense variant | C/T | snv | 8.0E-06 | 1 | ||
rs370624303 | 1.000 | 0.040 | 12 | 131910720 | missense variant | G/A | snv | 3.2E-05 | 2.1E-05 | 1 | |
rs200610853 | 1.000 | 0.040 | 7 | 141724247 | missense variant | G/A | snv | 4.0E-06 | 7.0E-06 | 1 |