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 | |
rs899127658 | 0.547 | 0.720 | 11 | 46739084 | missense variant | G/A;C | snv | 82 | |||
rs121918460 | 0.708 | 0.400 | 12 | 112450364 | missense variant | T/A;G | snv | 4.0E-06 | 27 | ||
rs1057518422 | 0.851 | 0.240 | 6 | 149378954 | stop gained | C/T | snv | 7 | |||
rs870142 | 0.851 | 0.120 | 4 | 4646320 | intron variant | C/G;T | snv | 7 | |||
rs16835979 | 0.851 | 0.120 | 4 | 4633549 | intron variant | C/A | snv | 0.20 | 6 | ||
rs6824295 | 0.851 | 0.120 | 4 | 4612553 | intron variant | C/T | snv | 0.20 | 6 | ||
rs1555223259 | 1.000 | 0.080 | 12 | 114355868 | stop gained | G/C | snv | 3 | |||
rs3729856 | 0.925 | 0.080 | 8 | 11757066 | missense variant | A/G | snv | 9.5E-02 | 9.0E-02 | 3 | |
rs1282433424 | 0.925 | 0.080 | 8 | 11755094 | missense variant | C/T | snv | 2 |