Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs1057519841 | 0.925 | 0.120 | 5 | 68295269 | missense variant | A/G | snv | 5 | |||
rs1057519732 | 0.827 | 0.160 | 15 | 66436824 | missense variant | C/A;T | snv | 6 | |||
rs1057519738 | 0.790 | 0.160 | 17 | 39725079 | missense variant | G/A | snv | 4.0E-06 | 7 | ||
rs1057519862 | 0.851 | 0.160 | 17 | 39723405 | missense variant | G/A | snv | 5 | |||
rs1057519893 | 0.790 | 0.160 | 12 | 56085070 | missense variant | G/A;T | snv | 8 | |||
rs1057519917 | 0.807 | 0.160 | 1 | 11124517 | missense variant | A/G;T | snv | 7 | |||
rs1057519931 | 0.827 | 0.160 | 3 | 179199141 | missense variant | G/C | snv | 6 | |||
rs1057519938 | 0.776 | 0.160 | 3 | 179203764 | missense variant | A/C;T | snv | 10 | |||
rs1057519939 | 0.776 | 0.160 | 3 | 179203763 | missense variant | A/C | snv | 10 | |||
rs1057519943 | 0.790 | 0.160 | 12 | 132676598 | missense variant | G/C;T | snv | 5 | |||
rs1057519944 | 0.882 | 0.160 | 12 | 132676599 | missense variant | G/A | snv | 5 | |||
rs1057519947 | 0.790 | 0.160 | 19 | 52212730 | missense variant | G/A | snv | 9 | |||
rs1057519999 | 0.763 | 0.160 | 17 | 7674247 | missense variant | T/C;G | snv | 12 | |||
rs121913284 | 0.776 | 0.160 | 3 | 179203765 | missense variant | T/A;G | snv | 10 | |||
rs749415085 | 0.807 | 0.160 | 3 | 179198937 | missense variant | C/A;G;T | snv | 7 | |||
rs759610249 | 0.790 | 0.160 | 4 | 152323032 | missense variant | C/T | snv | 8.0E-06 | 7.0E-06 | 8 | |
rs772110575 | 0.807 | 0.160 | 3 | 179198938 | missense variant | G/A;T | snv | 4.0E-06 | 6 | ||
rs876660807 | 0.763 | 0.160 | 17 | 7674248 | missense variant | T/C | snv | 12 | |||
rs1057519890 | 0.807 | 0.200 | 17 | 39723966 | missense variant | T/A | snv | 7 | |||
rs1057519936 | 0.776 | 0.200 | 3 | 179234284 | missense variant | A/G;T | snv | 11 | |||
rs1057519937 | 0.776 | 0.200 | 3 | 179234285 | missense variant | T/C | snv | 11 | |||
rs1057519940 | 0.752 | 0.200 | 3 | 179218308 | missense variant | G/T | snv | 13 | |||
rs1057519945 | 0.776 | 0.200 | 12 | 132673703 | missense variant | C/A;T | snv | 4 | |||
rs1057520009 | 0.790 | 0.200 | 2 | 61492337 | missense variant | C/T | snv | 4.4E-06 | 5 | ||
rs1057520010 | 0.882 | 0.200 | 2 | 61492336 | missense variant | T/A;G | snv | 5 |