Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs397507444 | 0.405 | 0.880 | 1 | 11794407 | missense variant | T/G | snv | 306 | |||
rs1801131 | 0.535 | 0.840 | 1 | 11794419 | missense variant | T/G | snv | 0.29 | 0.26 | 93 | |
rs234709 | 0.827 | 0.200 | 21 | 43066854 | intron variant | C/T | snv | 7 | |||
rs2124459 | 0.827 | 0.200 | 21 | 43055604 | 3 prime UTR variant | T/C | snv | 0.36 | 5 | ||
rs1060499603 | 0.882 | 0.040 | 8 | 71211239 | stop gained | C/A | snv | 3 | |||
rs397517920 | 0.882 | 0.040 | 8 | 71199371 | missense variant | A/G | snv | 3 | |||
rs4938016 | 0.925 | 0.120 | 11 | 113399293 | missense variant | G/A;C;T | snv | 1.7E-04; 0.64; 2.0E-03 | 2 | ||
rs234705 | 0.925 | 0.120 | 21 | 43063662 | intron variant | C/T | snv | 2 | |||
rs1076562 | 0.925 | 0.120 | 11 | 113425286 | intron variant | A/G | snv | 0.65 | 2 | ||
rs869025180 | 1.000 | 8 | 71299637 | splice donor variant | C/T | snv | 1 |