Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs575231506 | 0.925 | 0.160 | 4 | 2894667 | missense variant | C/A;T | snv | 4.1E-06; 4.1E-06 | 2 | ||
rs747418061 | 0.807 | 0.200 | 5 | 112828920 | missense variant | G/A | snv | 3.2E-05 | 7.0E-06 | 10 | |
rs1371086615 | 0.851 | 0.120 | 5 | 112828890 | missense variant | G/A | snv | 4.0E-06 | 7.0E-06 | 4 | |
rs765557332 | 0.851 | 0.120 | 5 | 112835075 | missense variant | G/A | snv | 7.0E-06 | 4 | ||
rs878853423 | 0.851 | 0.120 | 5 | 112837663 | missense variant | G/A | snv | 4 | |||
rs1431515214 | 0.925 | 0.080 | 5 | 112839790 | missense variant | G/A | snv | 4.0E-06 | 2 | ||
rs13306190 | 0.807 | 0.320 | 2 | 21032408 | missense variant | G/A;C;T | snv | 1.7E-04; 8.0E-06 | 7 | ||
rs777919630 | 0.623 | 0.680 | 21 | 43062358 | missense variant | G/A;T | snv | 8.0E-06; 4.0E-06 | 40 | ||
rs1188383936 | 0.524 | 0.760 | 11 | 46725976 | missense variant | C/T | snv | 8.0E-06 | 102 | ||
rs899127658 | 0.547 | 0.720 | 11 | 46739084 | missense variant | G/A;C | snv | 82 | |||
rs1799963 | 0.695 | 0.400 | 11 | 46739505 | 3 prime UTR variant | G/A | snv | 9.6E-03 | 25 | ||
rs1183194405 | 0.716 | 0.440 | 11 | 46719773 | missense variant | G/A;T | snv | 4.5E-06; 4.5E-06 | 19 | ||
rs552953108 | 0.724 | 0.200 | 11 | 46729529 | missense variant | G/A | snv | 1.6E-05 | 4.2E-05 | 16 | |
rs780225764 | 1.000 | 0.080 | 11 | 46726797 | missense variant | A/G | snv | 4.0E-06 | 2 | ||
rs779829591 | 0.827 | 0.320 | 1 | 94532395 | missense variant | G/A | snv | 4.0E-06 | 5 | ||
rs3789683 | 0.925 | 0.200 | 1 | 94530506 | missense variant | C/T | snv | 6.5E-03 | 1.0E-02 | 3 | |
rs751377893 | 0.574 | 0.680 | 1 | 169546513 | missense variant | T/C | snv | 4.0E-06 | 65 | ||
rs6025 | 0.637 | 0.560 | 1 | 169549811 | missense variant | C/T | snv | 1.8E-02 | 43 | ||
rs1312546120 | 0.807 | 0.160 | 1 | 169541191 | missense variant | T/C | snv | 4.0E-06 | 7 | ||
rs749785846 | 0.925 | 0.160 | 4 | 154568469 | synonymous variant | C/T | snv | 4.0E-06 | 2 | ||
rs2066865 | 0.807 | 0.240 | 4 | 154604124 | downstream gene variant | G/A | snv | 0.26 | 10 | ||
rs144246695 | 0.851 | 0.160 | 4 | 83310887 | missense variant | G/A | snv | 8.0E-06 | 4 | ||
rs911028477 | 1.000 | 0.080 | 16 | 27362773 | missense variant | G/A | snv | 2 | |||
rs77375493 | 0.458 | 0.760 | 9 | 5073770 | missense variant | G/A;T | snv | 3.5E-04 | 187 | ||
rs5918 | 0.683 | 0.480 | 17 | 47283364 | missense variant | T/C | snv | 0.12 | 0.13 | 26 |