CCDC149
coiled-coil domain containing 149
Known Variants31 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs193242333 | 4:24,810,022 | C/A | — | uncertain significance |
| rs1417993928 | 4:24,810,091 | G/A | — | uncertain significance |
| rs777579120 | 4:24,810,123 | T/G | — | uncertain significance |
| rs367730089 | 4:24,810,205 | T/C | — | uncertain significance |
| rs1395356610 | 4:24,810,317 | C/G | — | uncertain significance |
| rs61731836 | 4:24,810,333 | C/G | — | uncertain significance |
| rs866274450 | 4:24,810,361 | C/T | — | uncertain significance |
| rs200984075 | 4:24,810,384 | G/A | — | uncertain significance |
| rs556415780 | 4:24,810,393 | G/A | — | likely benign |
| rs763032516 | 4:24,811,451 | T/C | — | — |
| rs191079849 | 4:24,821,483 | T/C | — | uncertain significance |
| rs771408099 | 4:24,821,517 | C/G | — | uncertain significance |
| rs1450849190 | 4:24,821,520 | C/T | — | uncertain significance |
| rs369908357 | 4:24,821,523 | A/T | — | uncertain significance |
| rs934345013 | 4:24,824,191 | G/C | — | uncertain significance |
| rs1716147336 | 4:24,833,146 | T/C | — | uncertain significance |
| rs1716148240 | 4:24,833,156 | C/A | — | uncertain significance |
| rs200140047 | 4:24,836,629 | G/C | — | uncertain significance |
| rs1185226519 | 4:24,836,654 | T/C | — | uncertain significance |
| rs146803158 | 4:24,838,958 | C/T | — | uncertain significance |
| rs372455515 | 4:24,839,804 | G/T | — | uncertain significance |
| rs374446603 | 4:24,839,822 | C/T | — | uncertain significance |
| rs755220017 | 4:24,839,861 | C/T | — | uncertain significance |
| rs145660766 | 4:24,839,878 | A/G | — | uncertain significance |
| rs1170758716 | 4:24,839,894 | G/T | — | uncertain significance |
| rs777489891 | 4:24,854,716 | C/T | — | uncertain significance |
| rs201561233 | 4:24,854,721 | C/G | — | uncertain significance |
| rs1158875731 | 4:24,854,776 | T/C | — | uncertain significance |
| rs527390023 | 4:24,891,760 | C/G | — | — |
| rs746216101 | 4:24,896,628 | T/A | — | uncertain significance |
| rs6448318 | 4:24,953,939 | T/C | intron variant | — |
Gene information from NCBI Gene. Variant classifications from ClinVar.