Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs74142329 | 10 | 79190231 | intron variant | C/T | snv | 4.9E-02 | 1 | ||||
rs753270 | 1.000 | 0.080 | 10 | 79205218 | intron variant | T/A;C | snv | 1 | |||
rs77911174 | 0.925 | 0.080 | 10 | 79067076 | intron variant | A/G | snv | 5.4E-02 | 1 | ||
rs779933 | 10 | 79158760 | intron variant | G/A | snv | 0.36 | 2 | ||||
rs780151 | 10 | 79171724 | intron variant | G/A | snv | 0.32 | 1 | ||||
rs780159 | 10 | 79147390 | intron variant | A/C;G | snv | 2 | |||||
rs7914926 | 10 | 79170941 | intron variant | A/G | snv | 0.41 | 1 | ||||
rs7916441 | 10 | 79165820 | intron variant | G/C | snv | 0.39 | 2 |