Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs41311117 | 0.882 | 0.120 | 3 | 38550362 | missense variant | A/C;G;T | snv | 3.6E-05; 2.0E-03; 1.0E-05 | 3 | ||
rs199473639 | 1.000 | 0.080 | 3 | 38550469 | missense variant | A/C;G;T | snv | 1.6E-05; 4.1E-06; 4.1E-06 | 1 | ||
rs757532106 | 0.763 | 0.120 | 3 | 38550500 | stop gained | G/A | snv | 4.5E-05 | 4.9E-05 | 9 | |
rs41315493 | 0.851 | 0.120 | 3 | 38550521 | missense variant | C/A;T | snv | 6.6E-03; 9.7E-05 | 4 | ||
rs199473329 | 1.000 | 0.080 | 3 | 38550560 | stop gained | C/A;T | snv | 4.0E-06; 1.6E-05 | 1 | ||
rs199473637 | 1.000 | 0.080 | 3 | 38550569 | missense variant | C/T | snv | 2.8E-05 | 1.4E-05 | 1 | |
rs137854603 | 1.000 | 0.080 | 3 | 38550602 | missense variant | C/T | snv | 6.0E-05 | 2.8E-05 | 1 | |
rs864622270 | 1.000 | 0.080 | 3 | 38550665 | missense variant | C/A;T | snv | 4.0E-06 | 1 | ||
rs199473323 | 1.000 | 0.080 | 3 | 38550756 | missense variant | C/G | snv | 1 | |||
rs199473636 | 1.000 | 0.080 | 3 | 38550791 | missense variant | C/A;T | snv | 4.0E-06 | 1 | ||
rs199473322 | 0.925 | 0.080 | 3 | 38550823 | missense variant | C/G | snv | 2 | |||
rs199473320 | 0.882 | 0.120 | 3 | 38550878 | missense variant | G/C | snv | 6.0E-05 | 4.0E-04 | 3 | |
rs397514449 | 0.925 | 0.120 | 3 | 38550984 | protein altering variant | -/CAT | delins | 2 | |||
rs137854615 | 0.851 | 0.120 | 3 | 38550989 | missense variant | A/G | snv | 4 | |||
rs886037903 | 1.000 | 0.080 | 3 | 38551015 | frameshift variant | AG/- | del | 1 | |||
rs137854601 | 0.776 | 0.120 | 3 | 38551022 | stop gained | C/A;T | snv | 4.0E-06 | 10 | ||
rs199473634 | 0.925 | 0.120 | 3 | 38551036 | missense variant | G/A | snv | 4.0E-05 | 7.7E-05 | 2 | |
rs199473309 | 1.000 | 0.080 | 3 | 38551082 | missense variant | C/A | snv | 1 | |||
rs199473629 | 1.000 | 0.080 | 3 | 38551144 | missense variant | C/T | snv | 1 | |||
rs199473305 | 0.925 | 0.080 | 3 | 38551145 | missense variant | C/T | snv | 1.4E-05 | 2 | ||
rs199473304 | 1.000 | 0.080 | 3 | 38551154 | missense variant | C/T | snv | 1 | |||
rs193922726 | 1.000 | 0.080 | 3 | 38551188 | missense variant | G/A;C | snv | 6.0E-05 | 1 | ||
rs199473302 | 1.000 | 0.080 | 3 | 38551190 | missense variant | A/G | snv | 1 | |||
rs199473299 | 1.000 | 0.080 | 3 | 38551208 | missense variant | T/C | snv | 1 | |||
rs199473628 | 1.000 | 0.080 | 3 | 38551231 | missense variant | T/C | snv | 1 |