Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs2479409 | 1.000 | 0.040 | 1 | 55038977 | upstream gene variant | G/A | snv | 0.66 | 4 | ||
rs7025486 | 0.851 | 0.040 | 9 | 121660124 | intron variant | G/A | snv | 0.28 | 4 | ||
rs12133641 | 0.925 | 0.040 | 1 | 154455807 | intron variant | A/G | snv | 0.44 | 3 | ||
rs12695895 | 0.925 | 0.040 | 3 | 148725481 | intron variant | C/T | snv | 0.31 | 3 | ||
rs4916251 | 0.882 | 0.040 | 1 | 172377256 | intron variant | T/A | snv | 0.70 | 3 | ||
rs2234681 | 1.000 | 0.040 | 20 | 46008773 | upstream gene variant | ACACACACACACACACACACACAC/-;AC;ACAC;ACACAC;ACACACAC;ACACACACAC;ACACACACACAC;ACACACACACACAC;ACACACACACACACAC;ACACACACACACACACAC;ACACACACACACACACACAC;ACACACACACACACACACACAC;ACACACACACACACACACACACACAC;ACACACACACACACACACACACACACAC;ACACACACACACACACACACACACACACAC;ACACACACACACACACACACACACACACACAC;ACACACACACACACACACACACACACACACACAC | delins | 2 | |||
rs3827066 | 0.925 | 0.040 | 20 | 45957384 | intron variant | C/T | snv | 0.12 | 2 | ||
rs1036095 | 1.000 | 0.040 | 3 | 30620836 | intron variant | C/G | snv | 0.72 | 1 | ||
rs1057518075 | 1.000 | 0.040 | 2 | 188995061 | stop gained | C/T | snv | 1 | |||
rs10758278 | 1.000 | 0.040 | 9 | 34825306 | intron variant | G/A | snv | 0.53 | 1 | ||
rs10985349 | 1.000 | 0.040 | 9 | 121662964 | intron variant | C/T | snv | 0.17 | 1 | ||
rs13382862 | 1.000 | 0.040 | 2 | 20682689 | upstream gene variant | A/G;T | snv | 0.59 | 1 | ||
rs1385526 | 1.000 | 0.040 | 12 | 57138966 | intron variant | G/C | snv | 0.26 | 1 | ||
rs1418184396 | 1.000 | 0.040 | 17 | 1776722 | missense variant | C/T | snv | 4.0E-06 | 1 | ||
rs1419338705 | 1.000 | 0.040 | 7 | 74048163 | missense variant | C/T | snv | 7.0E-06 | 1 | ||
rs1795061 | 1.000 | 0.040 | 1 | 214235937 | intergenic variant | T/C;G | snv | 1 | |||
rs2070863 | 1.000 | 0.040 | 17 | 1745208 | missense variant | C/G;T | snv | 0.24 | 1 | ||
rs2306691 | 1.000 | 0.040 | 12 | 57145019 | missense variant | A/G | snv | 2.0E-05 | 2.1E-05 | 1 | |
rs2652106 | 1.000 | 0.040 | 5 | 83498217 | intron variant | G/T | snv | 0.39 | 1 | ||
rs2836411 | 1.000 | 0.040 | 21 | 38447907 | intron variant | C/A;T | snv | 1 | |||
rs3781590 | 1.000 | 0.040 | 11 | 68391684 | intron variant | G/A | snv | 0.35 | 1 | ||
rs58749629 | 1.000 | 0.040 | 20 | 45942678 | intron variant | G/A;T | snv | 0.13 | 1 | ||
rs6674171 | 1.000 | 0.040 | 1 | 154519207 | intron variant | A/G;T | snv | 0.19 | 1 | ||
rs766407419 | 1.000 | 0.040 | 17 | 1745008 | missense variant | T/C | snv | 8.0E-06 | 1.4E-05 | 1 | |
rs767169659 | 1.000 | 0.040 | 3 | 123733800 | missense variant | G/A | snv | 1.2E-05 | 1 |