Source: BEFREE
Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs63751273 | 0.645 | 0.280 | 17 | 46010389 | missense variant | C/T | snv | 39 | |||
rs63750424 | 0.677 | 0.240 | 17 | 46024061 | missense variant | C/T | snv | 1.6E-05 | 27 | ||
rs143624519 | 0.724 | 0.240 | 17 | 45991484 | missense variant | G/A;T | snv | 1.5E-03; 1.2E-05 | 17 | ||
rs63751438 | 0.776 | 0.120 | 17 | 46010388 | missense variant | C/T | snv | 16 | |||
rs242557 | 0.752 | 0.200 | 17 | 45942346 | intron variant | G/A | snv | 0.36 | 11 | ||
rs63749855 | 0.790 | 0.200 | 17 | 46014271 | missense variant | T/G | snv | 8 | |||
rs63750570 | 0.827 | 0.120 | 17 | 46018629 | missense variant | G/A | snv | 8 | |||
rs63750376 | 0.827 | 0.120 | 17 | 45996657 | missense variant | G/T | snv | 7 | |||
rs762046989 | 0.851 | 0.200 | 17 | 45971867 | missense variant | C/G | snv | 8.0E-06 | 5 | ||
rs9468 | 0.882 | 0.080 | 17 | 46024197 | 3 prime UTR variant | T/C | snv | 0.15 | 0.14 | 5 | |
rs1235948930 | 0.882 | 0.120 | 17 | 45983865 | missense variant | C/T | snv | 7.0E-06 | 4 | ||
rs63750072 | 1.000 | 0.080 | 17 | 45983493 | missense variant | A/G | snv | 4.0E-02 | 3.8E-02 | 3 | |
rs763459583 | 0.882 | 0.080 | 17 | 45987045 | missense variant | A/G;T | snv | 4.0E-06; 4.0E-06 | 3 | ||
rs2471738 | 0.882 | 0.160 | 17 | 45998697 | intron variant | C/T | snv | 0.18 | 3 | ||
rs1050210428 | 0.925 | 0.120 | 17 | 45983258 | missense variant | G/A | snv | 2 | |||
rs17649553 | 0.882 | 0.160 | 17 | 45917282 | intron variant | C/T | snv | 0.14 | 2 | ||
rs3785883 | 0.925 | 0.080 | 17 | 45977067 | non coding transcript exon variant | A/G | snv | 0.81 | 2 | ||
rs7521 | 0.925 | 0.080 | 17 | 46028029 | 3 prime UTR variant | A/C;G | snv | 2 | |||
rs1429412356 | 1.000 | 0.080 | 17 | 46023989 | missense variant | G/A | snv | 7.0E-06 | 1 | ||
rs1467967 | 1.000 | 0.080 | 17 | 45908813 | intron variant | G/A | snv | 0.66 | 1 | ||
rs1483785186 | 1.000 | 0.080 | 17 | 45996464 | missense variant | A/T | snv | 1 | |||
rs895897745 | 1.000 | 0.080 | 17 | 45991503 | missense variant | C/T | snv | 4.0E-06 | 7.0E-06 | 1 |