Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs2968857 | 1.000 | 0.080 | 7 | 150965242 | intron variant | C/T | snv | 0.70 | 2 | ||
rs1805120 | 0.882 | 0.080 | 7 | 150952443 | synonymous variant | G/A | snv | 0.30 | 0.26 | 3 | |
rs138776684 | 0.925 | 0.120 | 7 | 150957380 | missense variant | G/A | snv | 1.1E-03 | 6.3E-04 | 1 | |
rs199472918 | 0.882 | 0.120 | 7 | 150951738 | missense variant | A/G | snv | 7.2E-05 | 5.6E-05 | 2 | |
rs767910122 | 0.724 | 0.280 | 7 | 150948446 | frameshift variant | -/GTCCG | ins | 4.4E-05 | 17 | ||
rs781140785 | 0.925 | 0.040 | 7 | 150952801 | missense variant | C/T | snv | 1.2E-05 | 4.2E-05 | 2 | |
rs199473012 | 1.000 | 0.120 | 7 | 150947708 | missense variant | G/C | snv | 2.6E-05 | 4.2E-05 | 1 | |
rs62492438 | 1.000 | 0.080 | 7 | 150955422 | missense variant | G/A;C | snv | 7.1E-05 | 4.2E-05 | 1 | |
rs956828658 | 0.925 | 0.120 | 7 | 150958281 | missense variant | G/A | snv | 2.8E-05 | 2 | ||
rs199473014 | 0.925 | 0.120 | 7 | 150947684 | missense variant | G/T | snv | 2.1E-05 | 2 | ||
rs199473547 | 1.000 | 0.080 | 7 | 150945441 | missense variant | C/T | snv | 1.4E-05 | 1 | ||
rs121912512 | 0.882 | 0.120 | 7 | 150950311 | missense variant | C/T | snv | 4.0E-06 | 1.4E-05 | 2 | |
rs199473024 | 7 | 150947362 | missense variant | T/C | snv | 7.0E-06 | 2 | ||||
rs755834128 | 0.925 | 0.120 | 7 | 150952535 | missense variant | C/T | snv | 2.8E-05 | 7.0E-06 | 2 | |
rs1380382303 | 0.925 | 0.120 | 7 | 150950989 | synonymous variant | G/A | snv | 7.0E-06 | 2 | ||
rs794728448 | 0.724 | 0.280 | 7 | 150948445 | frameshift variant | CT/G | delins | 17 | |||
rs1805123 | 0.724 | 0.280 | 7 | 150948446 | missense variant | T/A;C;G | snv | 1.3E-05; 0.18; 8.4E-06 | 17 | ||
rs104894021 | 0.851 | 0.120 | 7 | 150951629 | missense variant | G/C;T | snv | 4 | |||
rs121912507 | 0.882 | 0.120 | 7 | 150951511 | missense variant | C/G;T | snv | 4 | |||
rs199472936 | 0.882 | 0.120 | 7 | 150951592 | missense variant | C/A;T | snv | 4 | |||
rs121912504 | 0.851 | 0.200 | 7 | 150951711 | missense variant | G/A | snv | 4 | |||
rs1254179611 | 1.000 | 0.120 | 7 | 150958295 | missense variant | G/A | snv | 3 | |||
rs773724817 | 0.925 | 0.160 | 7 | 150948861 | stop gained | G/A | snv | 4.0E-06 | 3 | ||
rs199473039 | 0.851 | 0.120 | 7 | 150951512 | missense variant | G/A;C;T | snv | 9.5E-05 | 3 | ||
rs199472954 | 0.882 | 0.120 | 7 | 150951514 | missense variant | A/G;T | snv | 3 |