Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs11552822 | 1.000 | 9 | 21971109 | missense variant | C/A;T | snv | 4.3E-06 | 2 | |||
rs140926412 | 0.925 | 12 | 7690177 | missense variant | G/A;T | snv | 2.0E-03; 4.0E-06 | 2 | |||
rs149925563 | 0.925 | 2 | 165941046 | missense variant | T/A | snv | 1.1E-03 | 7.0E-04 | 2 | ||
rs1085307958 | 0.925 | 7 | 2544920 | missense variant | A/G | snv | 2 | ||||
rs886039494 | 0.925 | 16 | 56336762 | missense variant | C/G;T | snv | 2 | ||||
rs398122955 | 0.925 | 4 | 125434349 | missense variant | G/A | snv | 4.0E-06 | 2 | |||
rs797045165 | 0.925 | 22 | 20991686 | missense variant | C/T | snv | 7.0E-06 | 2 | |||
rs776749939 | 0.925 | 5 | 179833777 | missense variant | C/T | snv | 6.0E-05 | 1.4E-05 | 2 | ||
rs146013446 | 0.925 | 4 | 105437964 | missense variant | C/T | snv | 4.9E-04 | 6.9E-04 | 2 | ||
rs587780076 | 17 | 7673743 | missense variant | C/A;T | snv | 8.0E-06; 8.0E-06 | 1 | ||||
rs774057024 | 11 | 94456331 | missense variant | C/T | snv | 1.6E-05 | 2.8E-05 | 1 | |||
rs748434421 | 11 | 94485928 | missense variant | T/A | snv | 4.0E-06 | 1.4E-05 | 1 | |||
rs200085146 | 11 | 94447287 | missense variant | C/T | snv | 2.0E-05 | 7.0E-06 | 1 | |||
rs869312784 | 5 | 112838674 | missense variant | A/G | snv | 1 | |||||
rs747621669 | 9 | 21970988 | missense variant | C/T | snv | 4.1E-06 | 1 | ||||
rs121913381 | 9 | 21971037 | missense variant | C/A;T | snv | 1 | |||||
rs137853213 | 1 | 40307477 | missense variant | TG/CA | mnv | 1 | |||||
rs587777600 | 19 | 10315996 | missense variant | T/A;G | snv | 1 | |||||
rs888630930 | 19 | 10310616 | missense variant | G/A | snv | 1 | |||||
rs121434328 | 12 | 95992772 | missense variant | C/A;T | snv | 3.6E-05 | 1 | ||||
rs121434329 | 12 | 95990472 | missense variant | G/A | snv | 2.8E-05 | 2.1E-05 | 1 | |||
rs121434327 | 12 | 95992778 | missense variant | C/G;T | snv | 1.2E-05; 3.2E-05 | 1 | ||||
rs121434330 | 12 | 95987153 | missense variant | C/G;T | snv | 2.0E-05 | 1 | ||||
rs28941786 | 1 | 70430388 | stop gained | C/G;T | snv | 8.0E-06; 4.0E-06 | 1 | ||||
rs116840786 | 3 | 8733962 | missense variant | C/A;T | snv | 1 |