Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs149617956 | 0.672 | 0.560 | 3 | 69964940 | missense variant | G/A | snv | 1.4E-03 | 1.6E-03 | 32 | |
rs77724903 | 0.672 | 0.280 | 10 | 43118460 | missense variant | A/G;T | snv | 4.0E-06; 2.1E-03 | 23 | ||
rs142441643 | 0.732 | 0.320 | 5 | 223509 | stop gained | C/T | snv | 2.0E-04 | 2.4E-04 | 15 | |
rs34677591 | 0.742 | 0.120 | 11 | 112086941 | missense variant | G/A | snv | 7.5E-03 | 7.0E-03 | 12 | |
rs80338844 | 0.776 | 0.280 | 11 | 112088939 | missense variant | C/T | snv | 2.0E-05 | 1.4E-05 | 10 | |
rs772551056 | 0.807 | 0.120 | 1 | 17044824 | missense variant | C/A;T | snv | 4.0E-06 | 9 | ||
rs80338845 | 0.807 | 0.240 | 11 | 112088971 | missense variant | G/T | snv | 7.0E-06 | 9 | ||
rs587782703 | 0.807 | 0.160 | 1 | 17053947 | splice donor variant | C/A;T | snv | 1.2E-05; 4.1E-06 | 8 | ||
rs80338842 | 0.790 | 0.280 | 11 | 112086910 | start lost | G/A;C | snv | 8 | |||
rs104894309 | 0.851 | 0.200 | 11 | 112086940 | stop gained | C/A;T | snv | 4.0E-06 | 7 | ||
rs587782604 | 0.827 | 0.120 | 1 | 17022684 | missense variant | C/A;T | snv | 4.0E-06; 4.0E-06 | 7 | ||
rs876658461 | 0.827 | 0.200 | 1 | 17023975 | stop gained | G/A | snv | 7 | |||
rs104894304 | 0.827 | 0.240 | 11 | 112094831 | missense variant | A/G | snv | 6 | |||
rs104894302 | 0.851 | 0.200 | 11 | 112089002 | missense variant | A/G;T | snv | 4.0E-06 | 5 | ||
rs1060503770 | 0.851 | 0.200 | 11 | 112094815 | stop gained | C/G;T | snv | 4.0E-06 | 5 | ||
rs1420960657 | 0.851 | 0.080 | 11 | 112093192 | missense variant | A/G | snv | 4 | |||
rs62624461 | 0.851 | 0.080 | 7 | 97117880 | missense variant | T/C | snv | 2.0E-02 | 1.8E-02 | 4 | |
rs942160050 | 0.882 | 0.080 | 1 | 161356685 | missense variant | C/A;G;T | snv | 4.0E-06 | 3 |