CCDC170
coiled-coil domain containing 170
Summary
The function of this gene and its encoded protein is not known. Several genome-wide association studies have implicated the region around this gene to be involved in breast cancer and bone mineral density, but no link to this specific gene has been found. [provided by RefSeq, May 2010]
Known Variants69 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs372621574 | 6:151,815,275 | C/A | — | uncertain significance |
| rs770061562 | 6:151,815,313 | C/A | — | uncertain significance |
| rs954238 | 6:151,844,443 | T/A | intron variant | — |
| rs9479055 | 6:151,847,967 | C/A | intron variant | — |
| rs11155795 | 6:151,851,339 | G/A | intron variant | — |
| rs564119648 | 6:151,857,454 | A/G | — | uncertain significance |
| rs1782580442 | 6:151,857,486 | A/G | — | uncertain significance |
| rs9371220 | 6:151,858,598 | C/T | intron variant | — |
| rs779271567 | 6:151,859,187 | A/C | — | uncertain significance |
| rs748562053 | 6:151,859,190 | T/A | — | uncertain significance |
| rs2486100611 | 6:151,859,229 | A/C | — | uncertain significance |
| rs755077457 | 6:151,859,285 | C/T | — | uncertain significance |
| rs771908138 | 6:151,859,337 | T/C | — | uncertain significance |
| rs2486101127 | 6:151,859,342 | A/G | — | uncertain significance |
| rs6923552 | 6:151,862,558 | T/G | — | — |
| rs200650721 | 6:151,865,707 | A/C | — | uncertain significance |
| rs776716381 | 6:151,865,789 | C/T | — | uncertain significance |
| rs200402314 | 6:151,869,451 | C/A | — | uncertain significance |
| rs371000974 | 6:151,869,542 | C/T | — | uncertain significance |
| rs767096405 | 6:151,869,586 | G/T | — | uncertain significance |
| rs372804729 | 6:151,869,596 | G/A | — | uncertain significance |
| rs760350115 | 6:151,869,605 | A/G | — | uncertain significance |
| rs9371538 | 6:151,872,963 | A/T | intron variant | — |
| rs755388816 | 6:151,894,387 | C/G | — | uncertain significance |
| rs55868409 | 6:151,894,567 | A/G | — | conflicting classifications of pathogenicity |
| rs2115089858 | 6:151,894,598 | T/C | — | uncertain significance |
| rs748873780 | 6:151,894,605 | C/A | — | uncertain significance |
| rs774072878 | 6:151,894,607 | G/A | — | likely benign |
| rs6909279 | 6:151,895,456 | G/T | — | — |
| rs12199746 | 6:151,896,523 | G/A | intron variant | — |
| rs1871859 | 6:151,898,506 | C/T | intron variant | — |
| rs1891002 | 6:151,900,047 | T/A | intron variant | — |
| rs4870044 | 6:151,901,409 | C/T | intron variant | — |
| rs4869739 | 6:151,901,802 | A/T | intron variant | — |
| rs200423775 | 6:151,907,028 | T/C | — | uncertain significance |
| rs75944154 | 6:151,907,109 | G/A | — | benign |
| rs199826959 | 6:151,907,127 | A/G | — | uncertain significance |
| rs2486198825 | 6:151,907,161 | C/A | — | uncertain significance |
| rs775579048 | 6:151,907,196 | G/A | — | uncertain significance |
| rs4869742 | 6:151,907,748 | C/T | intron variant | — |
| rs4869743 | 6:151,907,958 | T/C | intron variant | — |
| rs4869744 | 6:151,908,012 | T/A | — | — |
| rs4869745 | 6:151,908,076 | C/T | intron variant | — |
| rs6557155 | 6:151,910,126 | T/G | intron variant | — |
| rs9383929 | 6:151,911,872 | T/C | — | — |
| rs3757318 | 6:151,914,113 | G/A | regulatory region variant | — |
| rs961510157 | 6:151,914,251 | T/C | — | uncertain significance |
| rs550166524 | 6:151,914,317 | C/T | — | uncertain significance |
| rs35159094 | 6:151,914,385 | C/A | — | benign |
| rs781466443 | 6:151,917,494 | G/C | — | uncertain significance |
| rs183044234 | 6:151,917,524 | C/T | — | uncertain significance |
| rs369246635 | 6:151,917,567 | C/T | — | uncertain significance |
| rs201625561 | 6:151,917,596 | C/T | — | uncertain significance |
| rs754244719 | 6:151,917,657 | G/T | — | uncertain significance |
| rs954244273 | 6:151,917,677 | C/T | — | uncertain significance |
| rs12662670 | 6:151,918,856 | T/G | — | uncertain significance |
| rs149389640 | 6:151,925,507 | C/A | intron variant | — |
| rs1038304 | 6:151,933,175 | A/G | downstream gene variant | — |
| rs6929137 | 6:151,936,677 | G/A | missense variant | pathogenic |
| rs371502185 | 6:151,936,707 | G/A | — | uncertain significance |
| rs73780818 | 6:151,936,711 | C/A | — | benign |
| rs371023882 | 6:151,936,727 | A/C | — | uncertain significance |
| rs754697022 | 6:151,936,780 | A/T | — | uncertain significance |
| rs549368772 | 6:151,939,100 | G/T | — | uncertain significance |
| rs780980566 | 6:151,939,160 | A/T | — | uncertain significance |
| rs143566047 | 6:151,939,210 | C/G | — | likely benign |
| rs3734805 | 6:151,939,350 | A/C | upstream gene variant | uncertain significance |
| rs9383935 | 6:151,939,848 | C/T | upstream gene variant | benign |
| rs9383589 | 6:151,940,260 | A/G | — | uncertain significance |
Gene information from NCBI Gene. Variant classifications from ClinVar.