Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs1217691063 | 0.330 | 0.920 | 1 | 11796309 | missense variant | A/G | snv | 4.0E-06 | 7.0E-06 | 614 | |
rs17576 | 0.557 | 0.760 | 20 | 46011586 | missense variant | A/G | snv | 0.39 | 0.36 | 73 | |
rs16847548 | 0.807 | 0.120 | 1 | 162065484 | upstream gene variant | T/C | snv | 0.22 | 8 | ||
rs2106809 | 0.827 | 0.120 | X | 15599938 | intron variant | A/G | snv | 0.19 | 8 | ||
rs342293 | 0.882 | 0.040 | 7 | 106731773 | intron variant | C/G | snv | 0.42 | 7 | ||
rs12720459 | 0.807 | 0.160 | 11 | 2583535 | missense variant | C/A;G;T | snv | 7 | |||
rs10494366 | 0.851 | 0.200 | 1 | 162115895 | intron variant | G/T | snv | 0.54 | 7 | ||
rs12050217 | 0.827 | 0.160 | 14 | 96262416 | intron variant | A/G | snv | 0.21 | 6 | ||
rs12746200 | 0.851 | 0.160 | 1 | 186880054 | intron variant | A/G | snv | 7.3E-02 | 6 | ||
rs199472921 | 0.882 | 0.120 | 7 | 150951712 | missense variant | C/G;T | snv | 5 | |||
rs199472678 | 0.925 | 0.120 | 11 | 2445430 | missense variant | A/G | snv | 8.9E-06 | 3 | ||
rs2074238 | 1.000 | 0.120 | 11 | 2463573 | intron variant | T/A;C | snv | 3 | |||
rs199472742 | 1.000 | 0.120 | 11 | 2572982 | missense variant | G/T | snv | 2 | |||
rs11772585 | 7 | 91952189 | intron variant | C/T | snv | 0.11 | 1 | ||||
rs2282972 | 7 | 92037055 | intron variant | C/G;T | snv | 1 | |||||
rs7808587 | 7 | 91990782 | intron variant | G/A | snv | 0.57 | 1 | ||||
rs8234 | 11 | 2848878 | 3 prime UTR variant | A/G | snv | 0.45 | 0.38 | 1 | |||
rs10798 | 11 | 2848935 | 3 prime UTR variant | A/G | snv | 0.44 | 0.38 | 1 |