Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs12343867 | 0.790 | 0.200 | 9 | 5074189 | intron variant | T/C | snv | 0.25 | 9 | ||
rs10974944 | 0.882 | 0.160 | 9 | 5070831 | intron variant | C/G | snv | 0.25 | 4 | ||
rs1217691063 | 0.330 | 0.920 | 1 | 11796309 | missense variant | A/G | snv | 4.0E-06 | 7.0E-06 | 614 | |
rs77375493 | 0.458 | 0.760 | 9 | 5073770 | missense variant | G/A;T | snv | 3.5E-04 | 187 | ||
rs3742264 | 0.742 | 0.400 | 13 | 46073959 | missense variant | C/T | snv | 0.31 | 0.35 | 17 | |
rs199473373 | 0.882 | 0.120 | 17 | 70175283 | missense variant | C/T | snv | 3 | |||
rs1265538677 | 0.790 | 0.200 | 13 | 46055808 | synonymous variant | A/G | snv | 4.0E-06 | 10 |