Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs80338671 | 0.851 | 0.120 | 3 | 81642787 | missense variant | T/C;G | snv | 4.5E-04; 3.2E-04 | 5 | ||
rs201958741 | 0.851 | 0.120 | 3 | 81577999 | missense variant | C/T | snv | 3.3E-05 | 4.9E-05 | 4 | |
rs80338673 | 0.882 | 0.120 | 3 | 81577972 | missense variant | C/T | snv | 1.6E-05 | 4 | ||
rs192044702 | 0.882 | 0.120 | 3 | 81648854 | splice donor variant | A/G | snv | 8.9E-04 | 7.7E-04 | 3 | |
rs137852893 | 0.925 | 0.120 | 3 | 81642989 | missense variant | G/A | snv | 1.3E-05 | 2 | ||
rs369574719 | 1.000 | 0.120 | 3 | 81642988 | missense variant | C/T | snv | 3.0E-05 | 5.6E-05 | 1 | |
rs752711257 | 1.000 | 0.120 | 3 | 81586190 | missense variant | C/G;T | snv | 4.3E-06 | 1 |