Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs1057519880 | 0.925 | 0.080 | 19 | 49665875 | missense variant | C/T | snv | 4.0E-06 | 2 | ||
rs1057519885 | 0.925 | 0.080 | 20 | 20052443 | missense variant | G/A | snv | 2 | |||
rs137854599 | 0.882 | 0.080 | 9 | 21971093 | missense variant | C/G;T | snv | 2 | |||
rs267600971 | 0.882 | 0.080 | 6 | 31972346 | missense variant | G/A | snv | 2 | |||
rs868438023 | 0.882 | 0.080 | 15 | 40382906 | missense variant | C/T | snv | 2 | |||
rs1057519955 | 1.000 | 0.080 | 2 | 218584682 | missense variant | C/T | snv | 1 | |||
rs1805006 | 0.790 | 0.080 | 16 | 89919510 | missense variant | C/A;G | snv | 5.2E-03; 4.0E-06 | 1 | ||
rs267599211 | 0.882 | 0.080 | 2 | 218584683 | missense variant | C/T | snv | 1 | |||
rs121913386 | 0.807 | 0.120 | 9 | 21971018 | missense variant | G/A;T | snv | 6 | |||
rs121913512 | 0.851 | 0.120 | 4 | 54728055 | missense variant | A/C;G | snv | 6 | |||
rs1057519728 | 0.851 | 0.120 | 15 | 66435103 | missense variant | T/A;C;G | snv | 5 | |||
rs1057519757 | 0.882 | 0.120 | 5 | 68293310 | missense variant | G/A;C | snv | 5 | |||
rs1057519841 | 0.925 | 0.120 | 5 | 68295269 | missense variant | A/G | snv | 5 | |||
rs1057519874 | 0.807 | 0.120 | 7 | 6387261 | missense variant | C/A;T | snv | 4 | |||
rs1057519908 | 0.882 | 0.120 | 15 | 66435105 | missense variant | T/G | snv | 4 | |||
rs1057519948 | 0.851 | 0.120 | 7 | 6387262 | missense variant | C/T | snv | 4 | |||
rs1057519907 | 0.925 | 0.120 | 4 | 54728057 | missense variant | A/C | snv | 2 | |||
rs763733111 | 0.925 | 0.120 | 9 | 125149801 | missense variant | G/A | snv | 4.0E-06 | 2 | ||
rs759610249 | 0.790 | 0.160 | 4 | 152323032 | missense variant | C/T | snv | 8.0E-06 | 7.0E-06 | 8 | |
rs1057519917 | 0.807 | 0.160 | 1 | 11124517 | missense variant | A/G;T | snv | 7 | |||
rs1057519732 | 0.827 | 0.160 | 15 | 66436824 | missense variant | C/A;T | snv | 6 | |||
rs104894104 | 0.790 | 0.160 | 9 | 21971019 | missense variant | G/A;T | snv | 4 | |||
rs1057519910 | 0.851 | 0.160 | 19 | 4117551 | missense variant | A/C;T | snv | 4 | |||
rs1057519742 | 0.827 | 0.160 | 19 | 3118944 | missense variant | A/C;T | snv | 3 | |||
rs1057519786 | 0.882 | 0.160 | X | 47566722 | missense variant | C/G;T | snv | 3 |