Source: ALL
Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs63750009 | 0.851 | 0.120 | 14 | 73192760 | missense variant | A/C;G | snv | 5 | |||
rs63750050 | 0.925 | 0.080 | 14 | 73198106 | missense variant | T/G | snv | 5 | |||
rs63750886 | 0.851 | 0.080 | 14 | 73198072 | missense variant | C/G | snv | 5 | |||
rs63751106 | 0.827 | 0.080 | 14 | 73173643 | missense variant | T/A;C | snv | 5 | |||
rs1362575880 | 0.851 | 0.120 | 14 | 73192840 | missense variant | A/C | snv | 4.0E-06 | 4 | ||
rs63750001 | 0.851 | 0.080 | 14 | 73219188 | missense variant | C/T | snv | 4 | |||
rs63750004 | 0.851 | 0.080 | 14 | 73173655 | missense variant | T/A;C | snv | 4 | |||
rs63750444 | 0.882 | 0.080 | 14 | 73192745 | missense variant | G/A | snv | 4 | |||
rs63750929 | 0.882 | 0.080 | 14 | 73217177 | missense variant | G/T | snv | 4 | |||
rs63751024 | 0.851 | 0.120 | 14 | 73192793 | missense variant | T/C | snv | 4 | |||
rs63751254 | 0.851 | 0.160 | 14 | 73217210 | missense variant | A/G | snv | 4 | |||
rs63749885 | 0.882 | 0.080 | 14 | 73186859 | missense variant | C/T | snv | 3 | |||
rs63749925 | 0.882 | 0.080 | 14 | 73219191 | missense variant | C/T | snv | 3 | |||
rs63749961 | 0.925 | 0.080 | 14 | 73192772 | missense variant | T/G | snv | 3 | |||
rs63750265 | 0.882 | 0.080 | 14 | 73186869 | missense variant | T/A;C;G | snv | 3 | |||
rs63750391 | 0.882 | 0.160 | 14 | 73173665 | missense variant | G/A;C;T | snv | 3 | |||
rs63750800 | 0.882 | 0.080 | 14 | 73173585 | missense variant | G/A | snv | 3 | |||
rs63750815 | 0.882 | 0.080 | 14 | 73170974 | missense variant | G/T | snv | 3 | |||
rs63751141 | 0.882 | 0.080 | 14 | 73170984 | missense variant | G/C | snv | 3 | |||
rs866914724 | 0.882 | 0.080 | 14 | 73173685 | missense variant | T/C | snv | 3 | |||
rs906454643 | 0.882 | 0.080 | 14 | 73217219 | missense variant | T/C | snv | 4.0E-06 | 3 | ||
rs1446915570 | 0.925 | 0.080 | 14 | 73173623 | synonymous variant | A/T | snv | 4.0E-06 | 7.0E-06 | 2 | |
rs165932 | 0.925 | 0.080 | 14 | 73198145 | intron variant | G/A;T | snv | 0.61 | 2 | ||
rs200576075 | 0.925 | 0.080 | 14 | 73171031 | missense variant | C/T | snv | 2 | |||
rs63750353 | 0.925 | 0.080 | 14 | 73173630 | missense variant | A/G;T | snv | 2 |