Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs2281983 | 0.851 | 0.080 | 10 | 102231624 | missense variant | G/A;C;T | snv | 0.62; 8.3E-06 | 4 | ||
rs4919621 | 0.851 | 0.080 | 10 | 102238914 | intron variant | A/T | snv | 0.66 | 4 | ||
rs3758549 | 0.882 | 0.040 | 10 | 102244438 | upstream gene variant | G/A | snv | 0.14 | 3 | ||
rs1345514 | 1.000 | 0.040 | 7 | 155456455 | intron variant | C/T | snv | 0.29 | 1 | ||
rs3808330 | 1.000 | 0.040 | 7 | 155463312 | 3 prime UTR variant | T/C | snv | 0.23 | 1 | ||
rs1801334 | 0.851 | 0.040 | 6 | 161360193 | missense variant | C/T | snv | 2.5E-02 | 2.5E-02 | 4 | |
rs1189803871 | 1.000 | 0.040 | 6 | 161548929 | synonymous variant | G/A;C | snv | 4.0E-06 | 1 | ||
rs72480423 | 0.925 | 0.040 | 6 | 161569358 | missense variant | C/G;T | snv | 1.3E-04 | 2 | ||
rs751037529 | 0.925 | 0.040 | 6 | 161785793 | missense variant | C/G | snv | 1.2E-05 | 3 | ||
rs34424986 | 0.752 | 0.200 | 6 | 161785820 | missense variant | G/A;T | snv | 1.9E-03; 8.0E-06 | 10 | ||
rs150562946 | 0.882 | 0.040 | 6 | 161785877 | missense variant | G/A | snv | 4.2E-04 | 4.5E-04 | 3 | |
rs137853054 | 0.882 | 0.160 | 6 | 161973317 | missense variant | G/A;C;T | snv | 3.7E-04; 4.0E-06; 8.0E-06 | 4 | ||
rs755588390 | 0.851 | 0.160 | 6 | 162262672 | missense variant | T/C;G | snv | 7 | |||
rs74315360 | 0.925 | 0.040 | 1 | 20638104 | missense variant | C/A | snv | 3 | |||
rs74315359 | 0.882 | 0.040 | 1 | 20644651 | missense variant | C/T | snv | 2.0E-05 | 1.4E-05 | 3 | |
rs3738136 | 0.882 | 0.040 | 1 | 20645618 | missense variant | G/A | snv | 9.2E-02 | 5.0E-02 | 3 | |
rs45539432 | 0.851 | 0.040 | 1 | 20649109 | stop gained | C/T | snv | 4.0E-05 | 3.5E-05 | 5 | |
rs398122403 | 0.807 | 0.080 | 21 | 32695106 | missense variant | C/T | snv | 1.2E-05 | 11 | ||
rs139093920 | 1.000 | 0.040 | 22 | 38112241 | missense variant | C/T | snv | 8.0E-06 | 2.8E-05 | 1 | |
rs1171614044 | 1.000 | 0.040 | 22 | 38112243 | missense variant | T/C;G | snv | 1 | |||
rs199935023 | 0.882 | 0.040 | 22 | 38132917 | missense variant | C/A;T | snv | 4.9E-05; 3.6E-05 | 4 | ||
rs34637584 | 0.583 | 0.480 | 12 | 40340400 | missense variant | G/A | snv | 5.3E-04 | 3.6E-04 | 78 | |
rs34778348 | 0.742 | 0.120 | 12 | 40363526 | missense variant | G/A | snv | 1.7E-03 | 5.8E-04 | 15 | |
rs74315351 | 0.807 | 0.080 | 1 | 7962863 | missense variant | G/A | snv | 6 | |||
rs74315353 | 0.925 | 0.040 | 1 | 7965425 | missense variant | G/C | snv | 7.0E-06 | 2 |