Source: ALL
Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs243865 | 0.600 | 0.640 | 16 | 55477894 | intron variant | C/T | snv | 0.19 | 48 | ||
rs2285053 | 0.752 | 0.320 | 16 | 55478465 | intron variant | C/T | snv | 0.12 | 15 | ||
rs7201 | 0.925 | 0.160 | 16 | 55505702 | 3 prime UTR variant | A/C | snv | 0.37 | 4 | ||
rs371828436 | 1.000 | 0.120 | 16 | 55489798 | missense variant | G/A;T | snv | 4.0E-06 | 1 | ||
rs780391868 | 1.000 | 0.120 | 16 | 55491915 | missense variant | G/A;C;T | snv | 8.0E-06 | 1 |