Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs121434568 | 0.568 | 0.560 | 7 | 55191822 | missense variant | T/A;G | snv | 73 | |||
rs1057519847 | 0.570 | 0.560 | 7 | 55191821 | missense variant | CT/AG | mnv | 72 | |||
rs1057519848 | 0.570 | 0.560 | 7 | 55191822 | missense variant | TG/GT | mnv | 72 | |||
rs121434569 | 0.581 | 0.520 | 7 | 55181378 | missense variant | C/T | snv | 2.8E-05 | 5.6E-05 | 70 | |
rs397517132 | 0.623 | 0.280 | 7 | 55191846 | missense variant | A/T | snv | 48 | |||
rs2227983 | 0.658 | 0.520 | 7 | 55161562 | missense variant | G/A;C;T | snv | 0.29 | 31 | ||
rs121913444 | 0.724 | 0.160 | 7 | 55191831 | missense variant | T/A;C;G | snv | 18 | |||
rs1057519861 | 0.776 | 0.080 | 7 | 55181398 | missense variant | T/A | snv | 15 | |||
rs121913465 | 0.763 | 0.160 | 7 | 55181312 | missense variant | G/T | snv | 11 | |||
rs2072454 | 0.763 | 0.160 | 7 | 55146655 | synonymous variant | C/T | snv | 0.51 | 0.51 | 9 | |
rs28929495 | 0.807 | 0.120 | 7 | 55174014 | missense variant | G/A;C;T | snv | 9 | |||
rs397517108 | 0.790 | 0.120 | 7 | 55181312 | missense variant | GC/TT | mnv | 9 | |||
rs146795390 | 0.827 | 0.080 | 7 | 55191776 | missense variant | G/A | snv | 8.0E-06 | 7.0E-06 | 8 | |
rs748491031 | 0.827 | 0.120 | 7 | 55200384 | stop gained | C/G;T | snv | 1.2E-05 | 8 | ||
rs909797662 | 0.790 | 0.120 | 7 | 55191837 | missense variant | G/A | snv | 8 | |||
rs712829 | 0.776 | 0.120 | 7 | 55019062 | 5 prime UTR variant | G/C;T | snv | 8 | |||
rs1051753269 | 0.790 | 0.120 | 7 | 55174029 | missense variant | G/A | snv | 7.0E-06 | 7 | ||
rs11543848 | 0.790 | 0.240 | 7 | 55161562 | missense variant | G/A;C;T | snv | 7 | |||
rs1169803481 | 0.807 | 0.160 | 7 | 55198851 | missense variant | A/G | snv | 4.0E-06 | 7 | ||
rs149840192 | 0.807 | 0.080 | 7 | 55154129 | missense variant | C/A;T | snv | 7 | |||
rs886037891 | 0.790 | 0.160 | 7 | 55155917 | missense variant | G/T | snv | 4.0E-06 | 7 | ||
rs373129709 | 0.827 | 0.120 | 7 | 55019338 | missense variant | G/A;T | snv | 1.1E-04 | 7 | ||
rs121913428 | 0.827 | 0.120 | 7 | 55174015 | missense variant | G/A;C | snv | 6 | |||
rs1389500636 | 0.827 | 0.080 | 7 | 55156796 | missense variant | G/A | snv | 6 | |||
rs751295137 | 0.851 | 0.160 | 7 | 55152582 | missense variant | G/A | snv | 8.0E-06 | 7.0E-06 | 6 |