Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs5030805 | 0.790 | 0.280 | 3 | 10142086 | missense variant | G/A;T | snv | 7 | |||
rs121913308 | 0.827 | 0.120 | 10 | 43114492 | missense variant | A/C;G;T | snv | 6 | |||
rs36119840 | 0.807 | 0.280 | 5 | 37816010 | missense variant | G/A | snv | 2.3E-03 | 2.7E-03 | 6 | |
rs1060503770 | 0.851 | 0.200 | 11 | 112094815 | stop gained | C/G;T | snv | 4.0E-06 | 5 | ||
rs1416313401 | 0.827 | 0.160 | 8 | 109578004 | missense variant | A/G | snv | 4.1E-06 | 5 | ||
rs377767405 | 0.827 | 0.120 | 10 | 43114489 | missense variant | G/A;C;T | snv | 5 | |||
rs1183365192 | 0.851 | 0.160 | 10 | 43106550 | missense variant | C/T | snv | 7.0E-06 | 4 | ||
rs1188254133 | 0.851 | 0.240 | 6 | 43781990 | missense variant | T/G | snv | 7.0E-06 | 4 | ||
rs1420960657 | 0.851 | 0.080 | 11 | 112093192 | missense variant | A/G | snv | 4 | |||
rs34682185 | 0.851 | 0.120 | 10 | 43106382 | missense variant | G/A | snv | 6.3E-04 | 2.2E-04 | 4 | |
rs377767402 | 0.882 | 0.120 | 10 | 43113663 | missense variant | G/A | snv | 2.4E-05 | 2.8E-05 | 4 | |
rs5030827 | 0.882 | 0.200 | 3 | 10142097 | missense variant | G/A;C;T | snv | 4.4E-06 | 4 | ||
rs55846256 | 0.882 | 0.120 | 10 | 43114493 | missense variant | C/A;T | snv | 4.0E-06; 1.3E-04 | 4 | ||
rs62624461 | 0.851 | 0.080 | 7 | 97117880 | missense variant | T/C | snv | 2.0E-02 | 1.8E-02 | 4 | |
rs869025648 | 0.851 | 0.240 | 3 | 10146587 | synonymous variant | A/G | snv | 4 | |||
rs1400537035 | 0.882 | 0.200 | 7 | 101131931 | missense variant | C/A;G;T | snv | 3 | |||
rs267607170 | 0.882 | 0.200 | 3 | 10149814 | missense variant | A/G | snv | 3 | |||
rs377767430 | 0.882 | 0.080 | 10 | 43120192 | missense variant | A/C;G | snv | 3 | |||
rs397516444 | 0.882 | 0.200 | 3 | 10149808 | missense variant | G/A;T | snv | 4.0E-06 | 3 | ||
rs79661516 | 0.882 | 0.080 | 10 | 43105018 | missense variant | G/A | snv | 3 | |||
rs942160050 | 0.882 | 0.080 | 1 | 161356685 | missense variant | C/A;G;T | snv | 4.0E-06 | 3 | ||
rs374918502 | 0.925 | 0.080 | 1 | 156880056 | missense variant | C/T | snv | 6.0E-05 | 7.6E-06 | 2 | |
rs869025630 | 0.925 | 0.080 | 3 | 10142158 | missense variant | G/C;T | snv | 2 | |||
rs876659313 | 0.925 | 0.080 | 3 | 10146624 | missense variant | A/C;G | snv | 2 | |||
rs121913377 | 0.354 | 0.840 | 7 | 140753335 | missense variant | CA/AT;TT | mnv | 480 |