Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs755622 | 0.611 | 0.720 | 22 | 23894205 | intron variant | G/C | snv | 0.26 | 44 | ||
rs75996173 | 0.716 | 0.240 | 10 | 43114501 | missense variant | G/A;C;T | snv | 4.0E-06; 4.0E-06 | 21 | ||
rs76262710 | 0.724 | 0.280 | 10 | 43113648 | missense variant | T/A;C;G | snv | 4.0E-06; 4.0E-06 | 17 | ||
rs79781594 | 0.732 | 0.160 | 10 | 43113649 | missense variant | G/A;C;T | snv | 16 | |||
rs77939446 | 0.724 | 0.120 | 10 | 43113622 | missense variant | G/A;C;T | snv | 4.0E-06 | 15 | ||
rs1991517 | 0.752 | 0.240 | 14 | 81144239 | missense variant | G/C | snv | 0.90 | 0.91 | 13 | |
rs121913308 | 0.827 | 0.120 | 10 | 43114492 | missense variant | A/C;G;T | snv | 6 | |||
rs111033307 | 0.851 | 0.240 | 7 | 107694473 | missense variant | T/G | snv | 1.0E-04 | 7.7E-05 | 6 | |
rs2653349 | 0.882 | 0.120 | 6 | 55277539 | missense variant | A/G;T | snv | 0.84; 4.0E-06 | 5 | ||
rs377767395 | 0.882 | 0.120 | 10 | 43113613 | missense variant | A/G | snv | 4 | |||
rs377767402 | 0.882 | 0.120 | 10 | 43113663 | missense variant | G/A | snv | 2.4E-05 | 2.8E-05 | 4 | |
rs55846256 | 0.882 | 0.120 | 10 | 43114493 | missense variant | C/A;T | snv | 4.0E-06; 1.3E-04 | 4 | ||
rs28939086 | 0.925 | 0.160 | 7 | 107690220 | missense variant | A/C;G | snv | 2.0E-04; 4.0E-06 | 4 | ||
rs4774518 | 0.925 | 0.120 | 15 | 45117274 | stop gained | C/G;T | snv | 1.4E-04; 1.7E-02 | 3 | ||
rs180671269 | 1.000 | 0.120 | 15 | 45107450 | stop gained | T/A;C | snv | 6.8E-04; 4.0E-06 | 2 | ||
rs753012199 | 1.000 | 0.120 | 2 | 1477425 | missense variant | G/A | snv | 7.0E-06 | 2 | ||
rs368488511 | 15 | 45099748 | missense variant | C/G;T | snv | 1.9E-04 | 1 | ||||
rs140117073 | 4 | 7064176 | missense variant | C/A;G;T | snv | 4.0E-06; 5.3E-04 | 1 | ||||
rs80169463 | 4 | 3316336 | missense variant | G/A;C | snv | 1.2E-03; 4.0E-06 | 1 |