Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs113488022 | 0.351 | 0.840 | 7 | 140753336 | missense variant | A/C;G;T | snv | 4.0E-06 | 490 | ||
rs121913377 | 0.354 | 0.840 | 7 | 140753335 | missense variant | CA/AT;TT | mnv | 480 | |||
rs25487 | 0.441 | 0.800 | 19 | 43551574 | missense variant | T/C | snv | 0.68 | 0.71 | 205 | |
rs6265 | 0.436 | 0.760 | 11 | 27658369 | missense variant | C/T | snv | 0.19 | 0.15 | 272 | |
rs1801275 | 0.581 | 0.680 | 16 | 27363079 | missense variant | A/G | snv | 0.25 | 0.36 | 58 | |
rs61816761 | 0.658 | 0.640 | 1 | 152313385 | stop gained | G/A;T | snv | 9.4E-03; 8.0E-06 | 43 | ||
rs555743307 | 0.695 | 0.440 | 16 | 27342243 | missense variant | G/A;T | snv | 3.6E-05; 2.9E-04 | 20 | ||
rs2844484 | 0.807 | 0.320 | 6 | 31568447 | upstream gene variant | A/G | snv | 0.64 | 6 | ||
rs454886 | 0.763 | 0.280 | 5 | 112810420 | intron variant | A/G | snv | 0.26 | 10 | ||
rs33980500 | 0.742 | 0.200 | 6 | 111592059 | missense variant | C/T | snv | 8.6E-02 | 9.7E-02 | 14 | |
rs281875214 | 0.790 | 0.160 | 17 | 80183976 | missense variant | A/C | snv | 7 | |||
rs1347671835 | 0.827 | 0.160 | 16 | 88639888 | missense variant | C/A;G | snv | 4.3E-06 | 5 | ||
rs199473704 | 0.882 | 0.080 | 17 | 3524224 | missense variant | C/A;T | snv | 5 | |||
rs179363865 | 0.882 | 0.080 | X | 154563613 | missense variant | G/C | snv | 3 | |||
rs375557 | 0.882 | 0.080 | 13 | 41557730 | intergenic variant | G/A;C | snv | 3 | |||
rs1233255 | 1.000 | 0.040 | 2 | 189841366 | intron variant | A/C | snv | 0.27 | 1 |