Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs74315368 | 0.882 | 0.080 | 1 | 17022648 | missense variant | C/T | snv | 1.2E-05 | 1.4E-05 | 2 | |
rs772551056 | 0.807 | 0.120 | 1 | 17044824 | missense variant | C/A;T | snv | 4.0E-06 | 2 | ||
rs121917755 | 1.000 | 0.040 | 1 | 17028724 | missense variant | G/A;C | snv | 8.0E-06 | 1 | ||
rs138996609 | 0.882 | 0.080 | 1 | 17022685 | missense variant | G/A | snv | 8.0E-06 | 7.0E-06 | 1 | |
rs727504457 | 0.925 | 0.080 | 1 | 17033086 | missense variant | A/G | snv | 1 | |||
rs74315367 | 0.882 | 0.080 | 1 | 17024025 | missense variant | G/C | snv | 4.0E-06 | 1 | ||
rs74315370 | 0.882 | 0.080 | 1 | 17044825 | stop gained | G/A;C | snv | 1.6E-05 | 1 | ||
rs74315371 | 1.000 | 0.040 | 1 | 17028721 | missense variant | C/T | snv | 1 | |||
rs786202732 | 0.882 | 0.080 | 1 | 17024041 | missense variant | A/G | snv | 1 | |||
rs876658367 | 0.882 | 0.080 | 1 | 17024028 | missense variant | C/T | snv | 1 | |||
rs876659329 | 1.000 | 0.040 | 1 | 17044767 | missense variant | A/G;T | snv | 1 | |||
rs121908818 | 0.925 | 0.080 | 2 | 96265224 | stop gained | C/G;T | snv | 7.0E-06 | 1 | ||
rs121908819 | 1.000 | 0.040 | 2 | 96265174 | missense variant | C/T | snv | 2.0E-04 | 7.2E-04 | 1 | |
rs121908820 | 1.000 | 0.040 | 2 | 96265165 | missense variant | C/G | snv | 3.7E-05 | 3.5E-05 | 1 | |
rs121908823 | 1.000 | 0.040 | 2 | 96254974 | missense variant | C/T | snv | 6.7E-04 | 2.6E-03 | 1 | |
rs121908824 | 1.000 | 0.040 | 2 | 96254962 | missense variant | G/A;C;T | snv | 2.0E-05; 4.0E-06 | 1 | ||
rs121908827 | 1.000 | 0.040 | 2 | 96254107 | missense variant | A/G | snv | 1 | |||
rs121908828 | 1.000 | 0.040 | 2 | 96254106 | missense variant | C/A;T | snv | 4.0E-06 | 1 | ||
rs5030824 | 0.776 | 0.320 | 3 | 10149885 | missense variant | C/G | snv | 2.0E-05 | 4.2E-05 | 3 | |
rs1553619948 | 0.882 | 0.200 | 3 | 10146528 | missense variant | T/C | snv | 2 | |||
rs397516441 | 0.882 | 0.200 | 3 | 10149790 | missense variant | A/G | snv | 2 | |||
rs5030805 | 0.790 | 0.280 | 3 | 10142086 | missense variant | G/A;T | snv | 2 | |||
rs5030808 | 0.882 | 0.200 | 3 | 10142124 | missense variant | G/A;C;T | snv | 4.5E-06 | 2 | ||
rs5030809 | 0.776 | 0.320 | 3 | 10142139 | missense variant | T/C | snv | 1.3E-05 | 2 | ||
rs5030820 | 0.827 | 0.280 | 3 | 10149822 | missense variant | C/G;T | snv | 8.0E-06 | 2 |