Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs1057519916 | 0.882 | 0.160 | 1 | 11109320 | missense variant | T/A | snv | 4 | |||
rs1057519854 | 0.882 | 0.080 | 10 | 121488063 | missense variant | A/T | snv | 5 | |||
rs1057519891 | 0.851 | 0.160 | 12 | 56088557 | missense variant | G/A;T | snv | 4.0E-06 | 5 | ||
rs1057519892 | 0.851 | 0.160 | 12 | 56088558 | missense variant | A/T | snv | 5 | |||
rs1057519901 | 0.925 | 0.080 | 10 | 121498525 | missense variant | T/G | snv | 5 | |||
rs1057519915 | 0.851 | 0.160 | 1 | 11109318 | missense variant | A/C | snv | 5 | |||
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 | |||
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 | |||
rs121913476 | 0.851 | 0.080 | 10 | 121498520 | missense variant | A/C;T | snv | 5 | |||
rs1057519045 | 0.851 | 0.160 | 10 | 121498522 | missense variant | T/G | snv | 6 | |||
rs1057519738 | 0.790 | 0.160 | 17 | 39725079 | missense variant | G/A | snv | 4.0E-06 | 7 | ||
rs1057519890 | 0.807 | 0.200 | 17 | 39723966 | missense variant | T/A | snv | 7 | |||
rs121913470 | 0.776 | 0.200 | 17 | 39723967 | missense variant | T/C;G | snv | 7 | |||
rs1057519893 | 0.790 | 0.160 | 12 | 56085070 | missense variant | G/A;T | snv | 8 | |||
rs121913469 | 0.763 | 0.240 | 17 | 39723966 | missense variant | TT/CC | mnv | 8 | |||
rs786201419 | 0.790 | 0.160 | 17 | 7675180 | missense variant | C/A;T | snv | 8 | |||
rs786203071 | 0.776 | 0.240 | 17 | 7675181 | missense variant | T/A;G | snv | 8 | |||
rs1057519929 | 0.776 | 0.320 | 3 | 179199066 | missense variant | G/A | snv | 9 | |||
rs1057519941 | 0.776 | 0.240 | 3 | 179203761 | missense variant | T/C;G | snv | 9 | |||
rs1057519947 | 0.790 | 0.160 | 19 | 52212730 | missense variant | G/A | snv | 9 | |||
rs1057519926 | 0.776 | 0.200 | 3 | 179210293 | missense variant | A/T | snv | 10 | |||
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 |