Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs121912664 | 0.630 | 0.320 | 17 | 7670699 | missense variant | C/A;G;T | snv | 1.2E-05 | 40 | ||
rs121913343 | 0.611 | 0.520 | 17 | 7673803 | missense variant | G/A;C;T | snv | 1.2E-05 | 20 | ||
rs372201428 | 0.882 | 0.120 | 17 | 7676181 | missense variant | G/A;C | snv | 1.2E-05 | 3 | ||
rs375275361 | 0.827 | 0.120 | 17 | 7675054 | missense variant | A/G;T | snv | 1.2E-05; 4.0E-06 | 5 | ||
rs11540652 | 0.592 | 0.640 | 17 | 7674220 | missense variant | C/A;G;T | snv | 1.2E-05 | 20 | ||
rs587778718 | 1.000 | 0.080 | 17 | 7674959 | missense variant | G/A;C;T | snv | 4.0E-06; 1.2E-05; 4.0E-06 | 2 | ||
rs770374782 | 0.851 | 0.160 | 17 | 7673752 | missense variant | G/A;C | snv | 1.2E-05 | 4.2E-05 | 6 | |
rs201744589 | 0.882 | 0.240 | 17 | 7673728 | stop gained | C/A;G;T | snv | 4.0E-06; 1.2E-05 | 3 | ||
rs730881997 | 0.925 | 0.200 | 17 | 7675999 | missense variant | A/C;T | snv | 8.0E-06 | 4 | ||
rs375338359 | 0.882 | 0.200 | 17 | 7670684 | missense variant | C/G;T | snv | 8.0E-06 | 2 | ||
rs758781593 | 17 | 7675204 | missense variant | T/A;C;G | snv | 8.0E-06 | 2 | ||||
rs989692988 | 17 | 7676023 | splice donor variant | A/C | snv | 8.0E-06 | 1 | ||||
rs762846821 | 0.614 | 0.320 | 17 | 7675151 | missense variant | C/A;T | snv | 8.0E-06 | 56 | ||
rs587782705 | 0.807 | 0.280 | 17 | 7675157 | missense variant | G/A | snv | 8.0E-06 | 2 | ||
rs1060501206 | 17 | 7675056 | missense variant | C/T | snv | 8.0E-06 | 1 | ||||
rs587780728 | 1.000 | 0.120 | 17 | 7676224 | missense variant | C/G;T | snv | 4.0E-06; 8.0E-06 | 1 | ||
rs121912666 | 0.645 | 0.360 | 17 | 7674872 | missense variant | T/C;G | snv | 8.0E-06 | 13 | ||
rs1064794312 | 0.925 | 0.080 | 17 | 7674278 | missense variant | A/G | snv | 8.0E-06 | 2 | ||
rs876660829 | 17 | 7673598 | missense variant | G/C;T | snv | 8.0E-06 | 2 | ||||
rs750893877 | 0.807 | 0.320 | 17 | 7674258 | synonymous variant | G/A | snv | 8.0E-06 | 7 | ||
rs587780076 | 17 | 7673743 | missense variant | C/A;T | snv | 8.0E-06; 8.0E-06 | 1 | ||||
rs781490101 | 0.851 | 0.040 | 17 | 7673748 | missense variant | T/C | snv | 8.0E-06 | 5 | ||
rs1288373809 | 0.882 | 0.120 | 17 | 7673255 | synonymous variant | G/A | snv | 5.3E-06 | 5 | ||
rs768803947 | 0.882 | 0.080 | 17 | 7670624 | missense variant | C/A;T | snv | 4.0E-06; 4.0E-06 | 3 | ||
rs730882028 | 1.000 | 0.120 | 17 | 7670709 | missense variant | C/A;G;T | snv | 4.0E-06 | 2 |