KIAA0408
KIAA0408
Known Variants39 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs367597569 | 6:127,765,295 | T/C | — | uncertain significance |
| rs755809960 | 6:127,765,303 | G/A | — | uncertain significance |
| rs201926296 | 6:127,765,361 | G/A | — | uncertain significance |
| rs137996809 | 6:127,765,384 | C/T | — | uncertain significance |
| rs769086481 | 6:127,765,402 | T/C | — | uncertain significance |
| rs145129455 | 6:127,765,409 | C/T | — | likely benign |
| rs749497107 | 6:127,767,569 | G/A | — | uncertain significance |
| rs771096055 | 6:127,767,579 | C/G | — | uncertain significance |
| rs373762355 | 6:127,767,659 | C/T | — | uncertain significance |
| rs373508586 | 6:127,767,776 | A/G | — | uncertain significance |
| rs781112554 | 6:127,767,870 | T/C | — | uncertain significance |
| rs139745911 | 6:127,767,954 | G/A | missense variant | — |
| rs765834146 | 6:127,767,965 | T/A | — | uncertain significance |
| rs1294716654 | 6:127,768,058 | G/A | — | uncertain significance |
| rs1170285828 | 6:127,768,153 | C/A | — | uncertain significance |
| rs774400628 | 6:127,768,213 | C/G | — | likely benign |
| rs1447462142 | 6:127,768,220 | A/C | — | uncertain significance |
| rs531159220 | 6:127,768,386 | T/A | — | uncertain significance |
| rs2482316904 | 6:127,768,412 | G/C | — | uncertain significance |
| rs559066753 | 6:127,768,473 | A/G | — | uncertain significance |
| rs773852953 | 6:127,768,482 | C/T | — | uncertain significance |
| rs142527882 | 6:127,768,485 | C/T | — | uncertain significance |
| rs150954722 | 6:127,768,505 | A/C | — | uncertain significance |
| rs2482317617 | 6:127,768,559 | T/C | — | uncertain significance |
| rs2482318929 | 6:127,768,775 | T/C | — | uncertain significance |
| rs769550181 | 6:127,768,808 | T/C | — | likely benign |
| rs143121283 | 6:127,768,814 | T/C | — | likely benign |
| rs1015645047 | 6:127,768,866 | G/A | — | uncertain significance |
| rs769006833 | 6:127,771,031 | C/G | — | uncertain significance |
| rs147857938 | 6:127,771,327 | T/C | — | likely benign |
| rs570212497 | 6:127,771,364 | C/T | — | uncertain significance |
| rs756491042 | 6:127,771,377 | C/T | — | likely benign |
| rs779037731 | 6:127,771,386 | T/C | — | uncertain significance |
| rs140657174 | 6:127,771,400 | A/G | — | likely benign |
| rs765105326 | 6:127,771,406 | T/A | — | uncertain significance |
| rs2482327293 | 6:127,771,439 | A/G | — | uncertain significance |
| rs757724668 | 6:127,771,451 | C/T | — | uncertain significance |
| rs770313152 | 6:127,771,491 | G/A | — | uncertain significance |
| rs145321441 | 6:127,775,600 | G/A | intron variant | — |
Gene information from NCBI Gene. Variant classifications from ClinVar.