Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs1734907 | 0.925 | 0.080 | 7 | 100717894 | upstream gene variant | A/G | snv | 0.84 | 2 | ||
rs13126505 | 1.000 | 0.040 | 4 | 101944147 | intron variant | G/A | snv | 4.1E-02 | 1 | ||
rs13107325 | 0.776 | 0.520 | 4 | 102267552 | missense variant | C/A;T | snv | 4.0E-06; 4.5E-02 | 8 | ||
rs13001325 | 1.000 | 0.040 | 2 | 102322576 | intron variant | C/T | snv | 0.30 | 1 | ||
rs13015714 | 0.882 | 0.200 | 2 | 102355405 | intron variant | G/T | snv | 0.77 | 2 | ||
rs2058660 | 0.882 | 0.280 | 2 | 102437989 | intron variant | G/A | snv | 0.78 | 1 | ||
rs917997 | 0.701 | 0.480 | 2 | 102454108 | downstream gene variant | T/A;C | snv | 6 | |||
rs7705924 | 1.000 | 0.040 | 5 | 102611094 | intron variant | A/G | snv | 5.1E-02 | 1 | ||
rs74956615 | 0.807 | 0.160 | 19 | 10317045 | 3 prime UTR variant | T/A;C | snv | 1 | |||
rs12720356 | 0.752 | 0.360 | 19 | 10359299 | missense variant | A/C;G | snv | 6.1E-02; 4.0E-06 | 2 | ||
rs280519 | 0.752 | 0.320 | 19 | 10362257 | splice region variant | A/C;G | snv | 0.50 | 2 | ||
rs2304256 | 0.732 | 0.360 | 19 | 10364976 | missense variant | C/A | snv | 0.27 | 0.23 | 3 | |
rs11879191 | 1.000 | 0.040 | 19 | 10402235 | intron variant | G/A;C | snv | 1 | |||
rs6568421 | 1.000 | 0.040 | 6 | 105987150 | regulatory region variant | A/G | snv | 0.23 | 2 | ||
rs7746082 | 0.851 | 0.160 | 6 | 105987394 | regulatory region variant | G/A;C | snv | 3 | |||
rs12369214 | 0.807 | 0.120 | 12 | 106804833 | intron variant | G/A | snv | 0.41 | 1 | ||
rs12014762 | 0.882 | 0.080 | X | 106940440 | intron variant | C/T | snv | 0.14 | 1 | ||
rs2930047 | 0.925 | 0.040 | 5 | 10695414 | intron variant | T/C | snv | 0.49 | 1 | ||
rs6622126 | 0.851 | 0.080 | X | 106956972 | missense variant | G/A | snv | 0.58 | 1 | ||
rs4561177 | 0.807 | 0.120 | 11 | 110091706 | intron variant | A/G | snv | 0.36 | 1 | ||
rs11195128 | 1.000 | 0.040 | 10 | 110426390 | downstream gene variant | C/G;T | snv | 1 | |||
rs3184504 | 0.572 | 0.600 | 12 | 111446804 | missense variant | T/A;C;G | snv | 0.67 | 24 | ||
rs2903692 | 0.807 | 0.360 | 16 | 11144926 | intron variant | G/A | snv | 0.33 | 1 | ||
rs3851228 | 0.925 | 0.040 | 6 | 111526988 | intron variant | A/T | snv | 9.7E-02 | 1 | ||
rs653178 | 0.672 | 0.600 | 12 | 111569952 | intron variant | C/T | snv | 0.67 | 17 |