Source: ALL
Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs10507391 | 0.776 | 0.320 | 13 | 30737959 | intron variant | A/T | snv | 0.52 | 10 | ||
rs9551963 | 0.851 | 0.160 | 13 | 30758410 | intron variant | A/C;T | snv | 6 | |||
rs9579646 | 0.851 | 0.160 | 13 | 30736442 | intron variant | G/A;T | snv | 6 | |||
rs12429692 | 1.000 | 0.080 | 13 | 30738041 | intron variant | A/T | snv | 0.24 | 2 | ||
rs17222919 | 1.000 | 0.080 | 13 | 30734192 | intron variant | T/A;G | snv | 2 | |||
rs3803277 | 13 | 30744171 | non coding transcript exon variant | C/A | snv | 0.49 | 0.45 | 1 | |||
rs4769060 | 13 | 30763740 | intron variant | A/G | snv | 0.35 | 1 |