Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs28933979 | 0.587 | 0.600 | 18 | 31592974 | missense variant | G/A;C | snv | 1.0E-04 | 70 | ||
rs114925667 | 0.672 | 0.520 | 3 | 132675903 | missense variant | G/A;T | snv | 1.9E-03; 4.1E-06 | 64 | ||
rs104893877 | 0.614 | 0.360 | 4 | 89828149 | missense variant | C/T | snv | 59 | |||
rs121912438 | 0.605 | 0.520 | 21 | 31667299 | missense variant | G/A;C;T | snv | 1.2E-05; 8.0E-06 | 58 | ||
rs17849781 | 0.701 | 0.480 | 17 | 7673788 | missense variant | G/A;C;T | snv | 22 | |||
rs1475170339 | 0.732 | 0.240 | 16 | 1792325 | missense variant | T/C;G | snv | 18 | |||
rs141138948 | 0.807 | 0.120 | 9 | 37783993 | missense variant | T/C;G | snv | 4.1E-04 | 9 | ||
rs62643364 | 0.851 | 0.160 | 20 | 4699466 | synonymous variant | A/G;T | snv | 4.0E-06; 1.4E-04 | 7 | ||
rs1064039 | 0.827 | 0.200 | 20 | 23637790 | missense variant | C/G;T | snv | 0.20 | 6 | ||
rs1051169 | 0.851 | 0.200 | 21 | 46602317 | synonymous variant | C/A;G;T | snv | 0.65 | 5 | ||
rs1364050643 | 0.851 | 0.240 | 2 | 86232711 | missense variant | G/A | snv | 5 | |||
rs267607102 | 0.851 | 0.120 | 1 | 11022196 | missense variant | A/G | snv | 5 | |||
rs587777162 | 0.925 | 0.040 | 20 | 63495972 | missense variant | C/T | snv | 5 | |||
rs80356717 | 0.851 | 0.120 | 1 | 11018836 | missense variant | A/G | snv | 5 | |||
rs397514662 | 0.882 | 0.120 | 10 | 99716419 | missense variant | A/C;G | snv | 1.2E-05 | 4 | ||
rs398122370 | 0.925 | 0.160 | 20 | 4699851 | missense variant | G/C | snv | 4 | |||
rs121918413 | 1.000 | 0.120 | 5 | 151851470 | missense variant | G/T | snv | 3 | |||
rs74315322 | 1.000 | 0.040 | 1 | 154275165 | stop gained | C/T | snv | 3.6E-05 | 3 | ||
rs121913223 | 1.000 | 0.040 | 5 | 80633904 | missense variant | T/A | snv | 4.0E-06 | 2 | ||
rs1467252662 | 5 | 151851530 | missense variant | G/T | snv | 4.0E-06 | 2 | ||||
rs749191312 | 1.000 | 0.080 | 20 | 18497075 | synonymous variant | C/T | snv | 4.0E-06 | 2 | ||
rs756915170 | 19 | 49909654 | missense variant | T/C | snv | 4.0E-06 | 2 | ||||
rs771884087 | 1.000 | 0.080 | 20 | 45253726 | synonymous variant | T/C | snv | 2 | |||
rs374651285 | 4 | 73406645 | missense variant | G/A | snv | 1 | |||||
rs1457713736 | 8 | 11850867 | stop gained | C/T | snv | 7.0E-06 | 1 |