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 | 42 | |||
rs63750424 | 0.677 | 0.240 | 17 | 46024061 | missense variant | C/T | snv | 1.6E-05 | 30 | ||
rs63750756 | 0.716 | 0.200 | 17 | 46010324 | missense variant | T/G | snv | 2.6E-05 | 23 | ||
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 | |||
rs1386984902 | 0.790 | 0.160 | 21 | 26000095 | missense variant | G/A | snv | 9 | |||
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 | |||
rs63750416 | 0.851 | 0.120 | 17 | 46010373 | missense variant | A/C | snv | 7 | |||
rs63750512 | 0.827 | 0.160 | 17 | 46024010 | missense variant | G/A;C | snv | 1.2E-05 | 6 | ||
rs1314736087 | 0.851 | 0.120 | 8 | 109575782 | frameshift variant | GA/- | delins | 4.0E-06 | 5 | ||
rs63750349 | 0.851 | 0.200 | 17 | 45996638 | missense variant | C/G;T | snv | 4.0E-06 | 5 | ||
rs63750635 | 0.851 | 0.120 | 17 | 46014286 | missense variant | C/T | snv | 5 | |||
rs1189501362 | 0.882 | 0.120 | 3 | 119863583 | missense variant | G/A | snv | 7.0E-06 | 4 | ||
rs1205185774 | 0.882 | 0.120 | 14 | 77469161 | missense variant | C/T | snv | 4 | |||
rs1235948930 | 0.882 | 0.120 | 17 | 45983865 | missense variant | C/T | snv | 7.0E-06 | 4 | ||
rs63750129 | 0.882 | 0.120 | 17 | 45996612 | missense variant | A/C | snv | 4.0E-06 | 4 | ||
rs866604606 | 0.882 | 0.120 | 22 | 21772907 | missense variant | G/A | snv | 4 |