Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs115092681 | 1.000 | 0.080 | 3 | 174201323 | intron variant | G/A;C;T | snv | 2 | |||
rs141864436 | 1.000 | 0.080 | 2 | 50971652 | intron variant | G/A | snv | 1.6E-02 | 2 | ||
rs57504626 | 1.000 | 0.080 | 19 | 19609590 | intron variant | C/T | snv | 0.10 | 2 | ||
rs112284299 | 1.000 | 0.080 | 3 | 179850308 | intron variant | G/C | snv | 1.6E-02 | 2 | ||
rs6693796 | 1.000 | 0.080 | 1 | 170674137 | intron variant | T/C | snv | 7.7E-02 | 2 | ||
rs143838781 | 1.000 | 0.080 | 12 | 113940539 | intron variant | G/A | snv | 7.0E-03 | 2 | ||
rs75639901 | 1.000 | 0.080 | 6 | 25667803 | intron variant | A/G | snv | 4.8E-02 | 2 | ||
rs2631781 | 1.000 | 0.080 | 1 | 76128101 | intron variant | C/A;T | snv | 2 | |||
rs58847779 | 1.000 | 0.080 | 22 | 37736644 | intron variant | T/C | snv | 4.4E-02 | 2 | ||
rs7810240 | 1.000 | 0.080 | 7 | 150387372 | intron variant | T/C;G | snv | 2 | |||
rs13064411 | 3 | 113327793 | synonymous variant | A/G | snv | 0.12 | 9.9E-02 | 1 | |||
rs16914931 | 9 | 98330034 | intron variant | G/A | snv | 0.10 | 1 |