Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs398123316 | 0.851 | 0.160 | 10 | 87925530 | missense variant | A/G;T | snv | 8 | |||
rs869312702 | 0.827 | 0.160 | 9 | 128203609 | missense variant | G/A | snv | 10 | |||
rs1085308040 | 0.851 | 0.200 | 10 | 87961096 | missense variant | G/A;T | snv | 6 | |||
rs1553544133 | 0.851 | 0.200 | 2 | 199308845 | frameshift variant | TC/- | delins | 6 | |||
rs1085308046 | 0.790 | 0.240 | 10 | 87933160 | missense variant | T/C;G | snv | 9 | |||
rs587778779 | 0.807 | 0.240 | 2 | 218814379 | splice acceptor variant | G/A;T | snv | 14 | |||
rs121913294 | 0.776 | 0.280 | 10 | 87952143 | missense variant | G/A;C;T | snv | 8.0E-06 | 11 | ||
rs180177035 | 0.752 | 0.280 | 7 | 140801502 | missense variant | T/C | snv | 35 | |||
rs587784177 | 0.790 | 0.280 | 5 | 177283827 | missense variant | G/A | snv | 20 | |||
rs1557781252 | 0.742 | 0.320 | 1 | 153816414 | stop gained | G/A | snv | 33 | |||
rs281875196 | 0.851 | 0.320 | 9 | 2115927 | missense variant | G/A;C | snv | 9 | |||
rs121913355 | 0.641 | 0.520 | 7 | 140781602 | missense variant | C/A;G;T | snv | 4.0E-06 | 32 | ||
rs1563183492 | 0.708 | 0.520 | 7 | 70766248 | missense variant | C/T | snv | 32 | |||
rs1163944538 | 0.641 | 0.560 | 17 | 75494905 | frameshift variant | -/A | delins | 4.0E-06 | 73 | ||
rs121909224 | 0.627 | 0.560 | 10 | 87933147 | stop gained | C/G;T | snv | 1.2E-05 | 35 | ||
rs1352010373 | 0.641 | 0.560 | 17 | 75489265 | splice acceptor variant | G/C | snv | 73 | |||
rs61752717 | 0.583 | 0.840 | 16 | 3243407 | missense variant | T/A;C | snv | 2.8E-04 | 19 |