Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs772572695 | 1.000 | 0.040 | 1 | 151406427 | missense variant | C/A;T | snv | 2.5E-05 | 1 | ||
rs1858830 | 0.925 | 0.040 | 7 | 116672385 | 5 prime UTR variant | C/G | snv | 0.40 | 1 | ||
rs756691187 | 1.000 | 0.040 | 1 | 151404993 | missense variant | C/G | snv | 8.0E-06 | 7.0E-06 | 1 | |
rs782521991 | 0.925 | 0.040 | X | 154400848 | missense variant | C/G | snv | 3.5E-05 | 2.8E-05 | 1 | |
rs796053483 | 1.000 | 0.040 | 16 | 2060775 | missense variant | C/G | snv | 7.0E-06 | 1 | ||
rs121909224 | 0.627 | 0.560 | 10 | 87933147 | stop gained | C/G;T | snv | 1.2E-05 | 35 | ||
rs870142 | 0.851 | 0.120 | 4 | 4646320 | intron variant | C/G;T | snv | 2 | |||
rs6265 | 0.436 | 0.760 | 11 | 27658369 | missense variant | C/T | snv | 0.19 | 0.15 | 8 | |
rs1452075 | 1.000 | 0.040 | 3 | 62495388 | intron variant | C/T | snv | 0.73 | 4 | ||
rs797045050 | 0.807 | 0.120 | 2 | 240797715 | missense variant | C/T | snv | 4 | |||
rs11787216 | 1.000 | 0.040 | 8 | 141605122 | intron variant | C/T | snv | 0.26 | 2 | ||
rs121917893 | 0.807 | 0.160 | X | 71167508 | missense variant | C/T | snv | 2 | |||
rs1553518509 | 1.000 | 0.040 | 2 | 148468916 | stop gained | C/T | snv | 2 | |||
rs2230365 | 0.925 | 0.160 | 6 | 31557671 | synonymous variant | C/T | snv | 0.16 | 0.13 | 2 | |
rs1452048149 | 1.000 | 0.040 | 1 | 151404828 | missense variant | C/T | snv | 4.0E-06 | 1 | ||
rs1557870645 | 1.000 | 0.040 | 1 | 151407271 | missense variant | C/T | snv | 1 | |||
rs375712202 | 1.000 | 0.040 | 11 | 124923339 | splice donor variant | C/T | snv | 9.6E-05 | 1.4E-05 | 1 | |
rs4534 | 0.925 | 0.240 | 8 | 142879686 | missense variant | C/T | snv | 8.4E-02 | 4.1E-02 | 1 | |
rs61753971 | 0.925 | 0.120 | X | 154030546 | missense variant | C/T | snv | 1.3E-04 | 1.1E-04 | 1 | |
rs6824295 | 0.851 | 0.120 | 4 | 4612553 | intron variant | C/T | snv | 0.20 | 1 | ||
rs753214391 | 1.000 | 0.040 | 1 | 151406444 | missense variant | C/T | snv | 1.0E-05 | 2.1E-05 | 1 | |
rs754532606 | 1.000 | 0.040 | 1 | 151423526 | missense variant | C/T | snv | 8.0E-06 | 2.1E-05 | 1 | |
rs760059077 | 1.000 | 0.040 | 1 | 151405919 | missense variant | C/T | snv | 2.4E-05 | 2.1E-05 | 1 | |
rs763820362 | 1.000 | 0.040 | 1 | 151424045 | missense variant | C/T | snv | 2.4E-05 | 1 | ||
rs769236847 | 0.807 | 0.200 | 7 | 97869011 | missense variant | C/T | snv | 4.0E-06 | 3.5E-05 | 1 |