Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs1564617866 | 0.925 | 0.200 | 10 | 78000983 | missense variant | T/G | snv | 7 | |||
rs372445155 | 0.851 | 0.280 | 18 | 23554890 | missense variant | G/A | snv | 1.6E-05 | 2.1E-05 | 7 | |
rs80338700 | 0.851 | 0.200 | 16 | 8806398 | missense variant | C/G;T | snv | 4.0E-06; 2.4E-05 | 7 | ||
rs1114167423 | 0.882 | 0.240 | 9 | 32984704 | stop gained | T/A | snv | 6 | |||
rs137853066 | 0.827 | 0.320 | 1 | 160042339 | missense variant | C/G;T | snv | 8.0E-06 | 6 | ||
rs1555661648 | 0.882 | 0.240 | 18 | 26862297 | missense variant | C/G | snv | 6 | |||
rs1555889162 | 0.882 | 0.040 | 20 | 49374931 | missense variant | G/A;C | snv | 6 | |||
rs1561515242 | 1.000 | 0.080 | 5 | 111482938 | splice donor variant | G/A | snv | 6 | |||
rs775141057 | 0.882 | 0.120 | 12 | 106496115 | missense variant | C/A;T | snv | 4.0E-06 | 2.1E-05 | 6 | |
rs113994097 | 0.724 | 0.400 | 15 | 89323426 | missense variant | C/G | snv | 9.7E-04 | 7.9E-04 | 5 | |
rs121908212 | 0.732 | 0.160 | 19 | 13303877 | missense variant | G/A | snv | 5 | |||
rs141659620 | 0.882 | 0.160 | 16 | 89531961 | missense variant | G/A;C | snv | 8.3E-04; 8.0E-06 | 5 | ||
rs63750231 | 0.689 | 0.160 | 14 | 73198100 | missense variant | A/C;G | snv | 5 | |||
rs72547551 | 0.882 | 0.160 | 16 | 89550545 | missense variant | C/T | snv | 3.6E-05 | 1.5E-04 | 5 | |
rs748309520 | 0.882 | 0.160 | 16 | 89531903 | splice acceptor variant | G/A | snv | 1.6E-05 | 7.0E-06 | 5 | |
rs752989523 | 0.882 | 0.160 | 16 | 89553853 | stop gained | G/A;C | snv | 8.0E-06 | 5 | ||
rs754081544 | 0.925 | 0.080 | 10 | 100988947 | missense variant | A/G | snv | 1.6E-05 | 7.0E-06 | 5 | |
rs879253797 | 0.882 | 0.160 | 16 | 89556954 | missense variant | C/T | snv | 1.4E-05 | 5 | ||
rs1064797245 | 0.776 | 0.280 | 19 | 41970540 | missense variant | G/A | snv | 4 | |||
rs1565339091 | 1.000 | 0.200 | 11 | 124924796 | missense variant | T/C | snv | 4 | |||
rs28933385 | 0.695 | 0.320 | 20 | 4699818 | missense variant | G/A | snv | 4.0E-06 | 4 | ||
rs531630376 | 1.000 | 0.080 | 5 | 141955844 | stop gained | C/A | snv | 4.0E-06 | 4 | ||
rs773372123 | 0.851 | 0.160 | 16 | 1587209 | missense variant | C/T | snv | 2.0E-05 | 4 | ||
rs781934508 | 1.000 | 0.080 | 9 | 133352441 | splice region variant | C/A;T | snv | 2.4E-05 | 4 | ||
rs80358243 | 0.925 | 0.200 | 22 | 50083183 | intron variant | A/G;T | snv | 8.0E-06 | 4 |