Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs121913377 | 0.354 | 0.840 | 7 | 140753335 | missense variant | CA/AT;TT | mnv | 480 | |||
rs79781594 | 0.732 | 0.160 | 10 | 43113649 | missense variant | G/A;C;T | snv | 16 | |||
rs377767404 | 0.742 | 0.160 | 10 | 43114488 | missense variant | T/C | snv | 11 | |||
rs80338845 | 0.807 | 0.240 | 11 | 112088971 | missense variant | G/T | snv | 7.0E-06 | 9 | ||
rs104893824 | 0.776 | 0.320 | 3 | 10142181 | missense variant | T/A;C | snv | 8 | |||
rs77558292 | 0.776 | 0.160 | 10 | 43113621 | missense variant | T/A;C;G | snv | 8 | |||
rs80338842 | 0.790 | 0.280 | 11 | 112086910 | start lost | G/A;C | snv | 8 | |||
rs377767412 | 0.790 | 0.240 | 10 | 43114547 | synonymous variant | G/A | snv | 7 | |||
rs5030805 | 0.790 | 0.280 | 3 | 10142086 | missense variant | G/A;T | snv | 7 | |||
rs730882035 | 0.807 | 0.200 | 3 | 10149805 | missense variant | G/A | snv | 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 | |||
rs121913308 | 0.827 | 0.120 | 10 | 43114492 | missense variant | A/C;G;T | snv | 6 | |||
rs1060503757 | 0.882 | 0.080 | 1 | 17024024 | frameshift variant | G/- | delins | 5 | |||
rs1131691049 | 0.882 | 0.080 | 1 | 17054019 | start lost | T/A | snv | 5 | |||
rs1555187083 | 0.851 | 0.240 | 11 | 112089012 | splice donor variant | G/A;T | snv | 5 | |||
rs377767405 | 0.827 | 0.120 | 10 | 43114489 | missense variant | G/A;C;T | snv | 5 | |||
rs397516833 | 0.882 | 0.080 | 1 | 17028737 | splice acceptor variant | C/G | snv | 5 | |||
rs397516836 | 0.882 | 0.080 | 1 | 17024015 | stop gained | C/A;T | snv | 5 | |||
rs587776649 | 0.851 | 0.240 | 11 | 112087861 | frameshift variant | G/- | del | 5 | |||
rs587781270 | 0.882 | 0.080 | 1 | 17033058 | splice donor variant | A/T | snv | 5 | |||
rs786201063 | 0.882 | 0.080 | 1 | 17033059 | splice donor variant | C/T | snv | 5 | |||
rs786201161 | 0.882 | 0.080 | 1 | 17024076 | splice acceptor variant | T/C | snv | 5 | |||
rs786202732 | 0.882 | 0.080 | 1 | 17024041 | missense variant | A/G | snv | 5 | |||
rs786203251 | 0.882 | 0.080 | 1 | 17022649 | missense variant | G/A;T | snv | 5 |