Source: CURATED
Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs121913595 | 0.742 | 0.160 | 1 | 161306785 | missense variant | G/A;T | snv | 10 | |||
rs121913603 | 0.732 | 0.160 | 1 | 161306722 | missense variant | T/C;G | snv | 2.0E-05 | 8 | ||
rs121913597 | 0.827 | 0.160 | 1 | 161307268 | missense variant | T/A | snv | 4 | |||
rs121913599 | 0.882 | 0.080 | 1 | 161306763 | missense variant | G/T | snv | 2 | |||
rs121913602 | 0.851 | 0.120 | 1 | 161307308 | missense variant | T/A | snv | 2 | |||
rs1553259643 | 0.925 | 0.080 | 1 | 161306719 | frameshift variant | TACA/- | delins | 2 | |||
rs1553259662 | 0.827 | 0.200 | 1 | 161306821 | missense variant | A/G | snv | 2 | |||
rs1553259703 | 0.925 | 0.080 | 1 | 161306900 | stop gained | G/A | snv | 2 | |||
rs281865128 | 0.882 | 0.080 | 1 | 161306426 | missense variant | C/G;T | snv | 2 | |||
rs572010627 | 0.851 | 0.160 | 1 | 161306738 | missense variant | A/C;T | snv | 8.0E-06 | 2 | ||
rs863225026 | 0.925 | 0.080 | 1 | 161305973 | splice acceptor variant | TCTGGGGGAGGGGCG/- | delins | 2 | |||
rs121913608 | 0.925 | 0.080 | 1 | 161306789 | missense variant | C/T | snv | 1 | |||
rs1553259760 | 0.925 | 0.080 | 1 | 161307299 | missense variant | T/C | snv | 1 | |||
rs760730366 | 1.000 | 0.080 | 1 | 161307356 | frameshift variant | GGGAGCCC/- | delins | 1.2E-05 | 1 | ||
rs879254038 | 0.925 | 0.080 | 1 | 161306800 | missense variant | T/C | snv | 1 |