Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs243865 | 0.600 | 0.640 | 16 | 55477894 | intron variant | C/T | snv | 0.19 | 48 | ||
rs1219648 | 0.716 | 0.320 | 10 | 121586676 | intron variant | A/G;T | snv | 17 | |||
rs2252070 | 0.752 | 0.320 | 11 | 102955810 | upstream gene variant | C/T | snv | 0.68 | 13 | ||
rs12532 | 0.790 | 0.200 | 4 | 4863419 | 3 prime UTR variant | A/G | snv | 0.36 | 10 | ||
rs121908568 | 0.807 | 0.160 | 17 | 65536495 | stop gained | G/A | snv | 9 | |||
rs987525 | 0.807 | 0.160 | 8 | 128933908 | intron variant | C/A | snv | 0.31 | 7 | ||
rs3178250 | 0.827 | 0.080 | 20 | 6779554 | 3 prime UTR variant | T/C | snv | 0.21 | 5 | ||
rs8049367 | 0.851 | 0.240 | 16 | 3930444 | downstream gene variant | T/C | snv | 0.37 | 4 | ||
rs1095 | 0.925 | 0.080 | 4 | 4863211 | 3 prime UTR variant | C/T | snv | 1.5E-02 | 2 | ||
rs11001553 | 0.925 | 0.080 | 10 | 52313141 | intron variant | C/T | snv | 0.12 | 2 | ||
rs28933970 | 0.925 | 0.080 | 14 | 36662954 | missense variant | T/C | snv | 2 | |||
rs483352804 | 0.925 | 0.080 | X | 70035389 | missense variant | G/A;T | snv | 2 | |||
rs861019 | 0.925 | 0.120 | 1 | 209802041 | splice region variant | A/G | snv | 0.44 | 2 | ||
rs1292564852 | 1.000 | 4 | 1805414 | missense variant | C/T | snv | 7.0E-06 | 1 | |||
rs1444216093 | 1.000 | 4 | 5632031 | missense variant | G/A;C | snv | 1 | ||||
rs15705 | 1.000 | 20 | 6779333 | 3 prime UTR variant | A/C;T | snv | 1 | ||||
rs17015215 | 1.000 | 1 | 209790735 | missense variant | C/T | snv | 1 | ||||
rs2268626 | 1.000 | 14 | 75978424 | intron variant | C/T | snv | 0.80 | 1 | |||
rs317250 | 1.000 | 2 | 76036546 | intron variant | C/T | snv | 0.96 | 1 | |||
rs7802 | 1.000 | 1 | 209785814 | 3 prime UTR variant | A/G | snv | 7.0E-04 | 1 | |||
rs758420403 | 1.000 | 4 | 5689210 | missense variant | A/C | snv | 4.0E-06 | 1 | |||
rs104894562 | 0.882 | 0.200 | 17 | 28529157 | stop gained | C/T | snv | 4.0E-06 | 7.0E-06 | 3 | |
rs1315861554 | 0.925 | 0.120 | 18 | 3457392 | missense variant | C/T | snv | 4.0E-06 | 2 | ||
rs116998555 | 0.882 | 0.080 | 2 | 218890118 | missense variant | C/A;T | snv | 4.0E-06; 1.9E-03 | 3 | ||
rs104894469 | 0.925 | 0.080 | 14 | 36663043 | missense variant | G/A;T | snv | 4.0E-06 | 2 |