Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs387906698 | 0.827 | 0.040 | 7 | 142751919 | missense variant | C/A;T | snv | 4.0E-06; 7.2E-05 | 8 | ||
rs61734659 | 0.790 | 0.160 | 7 | 142774035 | missense variant | G/A | snv | 1.4E-02 | 8 | ||
rs748405415 | 0.790 | 0.160 | 7 | 142773993 | stop gained | G/A;T | snv | 8 | |||
rs886037774 | 0.882 | 0.120 | 8 | 19955993 | missense variant | T/C | snv | 7 | |||
rs886037775 | 0.882 | 0.120 | 8 | 19960948 | missense variant | A/T | snv | 7 | |||
rs202003805 | 0.827 | 0.120 | 7 | 142750561 | missense variant | C/T | snv | 9.0E-05 | 6 | ||
rs57749775 | 0.851 | 0.080 | 12 | 52904822 | missense variant | A/G;T | snv | 1.7E-03; 4.0E-06 | 6 | ||
rs76371115 | 0.807 | 0.160 | 7 | 117531041 | missense variant | A/C;G;T | snv | 8.0E-06 | 6 | ||
rs121909293 | 0.851 | 0.080 | 1 | 15445717 | missense variant | C/T | snv | 4.4E-03 | 3.8E-03 | 5 | |
rs12688220 | 0.827 | 0.200 | X | 107001537 | upstream gene variant | C/T | snv | 0.19 | 5 | ||
rs140808909 | 0.851 | 0.120 | 19 | 44909080 | missense variant | G/A | snv | 2.0E-04 | 5.6E-05 | 5 | |
rs42490 | 0.882 | 0.160 | 8 | 89766285 | intron variant | G/A | snv | 0.60 | 5 | ||
rs7057398 | 0.827 | 0.080 | X | 106901299 | intron variant | T/C | snv | 0.41 | 5 | ||
rs118204082 | 0.851 | 0.120 | 8 | 19955863 | missense variant | C/G;T | snv | 1.5E-04 | 4 | ||
rs6622126 | 0.851 | 0.080 | X | 106956972 | missense variant | G/A | snv | 0.58 | 4 | ||
rs111033567 | 0.882 | 0.040 | 7 | 142750582 | missense variant | A/G | snv | 3 | |||
rs111033568 | 0.882 | 0.040 | 7 | 142751937 | missense variant | C/G;T | snv | 2.0E-05 | 3 | ||
rs11971167 | 0.882 | 0.160 | 7 | 117642528 | missense variant | G/A;T | snv | 1.3E-03 | 3 | ||
rs12008279 | 0.882 | 0.080 | X | 106917472 | intron variant | A/G;T | snv | 3 | |||
rs12014762 | 0.882 | 0.080 | X | 106940440 | intron variant | C/T | snv | 0.14 | 3 | ||
rs145844329 | 0.882 | 0.120 | 8 | 143215486 | missense variant | G/A;C | snv | 2.5E-05; 8.5E-04 | 3 | ||
rs149089920 | 0.925 | 0.120 | 8 | 19962134 | missense variant | G/A | snv | 6.0E-05 | 2.1E-04 | 3 | |
rs190853081 | 0.925 | 0.080 | 19 | 44909083 | missense variant | G/A | snv | 2.0E-04 | 5.6E-05 | 3 | |
rs3809849 | 0.882 | 0.120 | 17 | 4555303 | missense variant | G/C;T | snv | 0.21; 3.1E-05 | 3 | ||
rs397508139 | 0.882 | 0.160 | 7 | 117540237 | missense variant | T/A;C | snv | 4.0E-06; 4.0E-06 | 3 |