Source: BEFREE
Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs12951053 | 0.732 | 0.160 | 17 | 7674089 | intron variant | A/C | snv | 0.10 | 14 | ||
rs2078486 | 0.882 | 0.080 | 17 | 7679765 | intron variant | G/A;C | snv | 3 | |||
rs1429743956 | 0.882 | 0.080 | 17 | 7674906 | stop gained | T/A;C | snv | 3 | |||
rs1042522 | 0.426 | 0.800 | 17 | 7676154 | missense variant | G/C;T | snv | 0.67 | 242 | ||
rs878854066 | 0.439 | 0.800 | 17 | 7676153 | missense variant | GG/AC | mnv | 213 | |||
rs762846821 | 0.614 | 0.320 | 17 | 7675151 | missense variant | C/A;T | snv | 8.0E-06 | 56 | ||
rs28934576 | 0.554 | 0.600 | 17 | 7673802 | missense variant | C/A;G;T | snv | 4.0E-06; 1.6E-05 | 47 | ||
rs28934578 | 0.605 | 0.600 | 17 | 7675088 | missense variant | C/A;T | snv | 4.0E-06 | 36 | ||
rs1057520001 | 0.677 | 0.360 | 17 | 7674886 | missense variant | A/C;G | snv | 23 | |||
rs886039484 | 0.641 | 0.440 | 17 | 7674888 | missense variant | T/C;G | snv | 23 | |||
rs1057519975 | 0.649 | 0.480 | 17 | 7675209 | missense variant | A/C;G;T | snv | 21 | |||
rs11540652 | 0.592 | 0.640 | 17 | 7674220 | missense variant | C/A;G;T | snv | 1.2E-05 | 20 | ||
rs121912654 | 0.683 | 0.400 | 17 | 7675143 | missense variant | C/A;T | snv | 4.0E-05 | 19 | ||
rs760043106 | 0.645 | 0.440 | 17 | 7674947 | missense variant | A/C;G;T | snv | 16 | |||
rs1800371 | 0.742 | 0.240 | 17 | 7676230 | missense variant | G/A;T | snv | 1.2E-03 | 15 | ||
rs375275361 | 0.827 | 0.120 | 17 | 7675054 | missense variant | A/G;T | snv | 1.2E-05; 4.0E-06 | 5 | ||
rs587782596 | 0.807 | 0.200 | 17 | 7675071 | missense variant | G/A;T | snv | 5 | |||
rs1019340046 | 0.882 | 0.080 | 17 | 7674225 | missense variant | C/T | snv | 4 | |||
rs267605076 | 0.851 | 0.160 | 17 | 7674859 | missense variant | C/A;T | snv | 4.0E-06 | 4 | ||
rs1057519984 | 0.882 | 0.080 | 17 | 7673777 | missense variant | G/C;T | snv | 3 | |||
rs375573770 | 0.882 | 0.080 | 17 | 7670682 | missense variant | C/G | snv | 7.0E-06 | 3 | ||
rs483352697 | 0.695 | 0.480 | 17 | 7674944 | missense variant | C/A;G;T | snv | 4.0E-06 | 3 | ||
rs587781991 | 0.724 | 0.240 | 17 | 7675208 | missense variant | C/A;T | snv | 3 | |||
rs587782769 | 0.882 | 0.080 | 17 | 7676155 | missense variant | G/A;C;T | snv | 1.6E-05; 1.2E-05; 4.0E-06 | 3 | ||
rs863224682 | 1.000 | 0.080 | 17 | 7669655 | missense variant | C/A;T | snv | 4.0E-06 | 2 |