CCDC171
coiled-coil domain containing 171
Known Variants123 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs368515656 | 9:15,564,105 | A/G | — | uncertain significance |
| rs2538525000 | 9:15,571,636 | C/T | — | uncertain significance |
| rs141895202 | 9:15,571,755 | G/A | — | uncertain significance |
| rs772190980 | 9:15,578,850 | G/T | — | uncertain significance |
| rs376424195 | 9:15,578,857 | A/T | — | uncertain significance |
| rs79217038 | 9:15,578,863 | G/A | — | likely benign |
| rs756983997 | 9:15,578,887 | A/T | — | uncertain significance |
| rs115940611 | 9:15,578,890 | T/C | — | benign |
| rs143875575 | 9:15,578,896 | A/T | — | uncertain significance |
| rs763638459 | 9:15,578,929 | A/T | — | uncertain significance |
| rs200525843 | 9:15,578,961 | G/A | — | uncertain significance |
| rs142125441 | 9:15,578,967 | C/T | — | uncertain significance |
| rs2538972793 | 9:15,591,448 | G/A | — | uncertain significance |
| rs2538972961 | 9:15,591,456 | G/C | — | uncertain significance |
| rs537658743 | 9:15,591,465 | T/G | — | uncertain significance |
| rs1460617237 | 9:15,591,478 | A/G | — | uncertain significance |
| rs763777871 | 9:15,591,506 | A/G | — | likely benign |
| rs372596980 | 9:15,594,051 | A/G | — | uncertain significance |
| rs752038797 | 9:15,594,091 | G/A | — | uncertain significance |
| rs755383791 | 9:15,594,120 | C/G | — | uncertain significance |
| rs140382641 | 9:15,597,149 | C/T | — | — |
| rs2457263 | 9:15,599,350 | C/A | — | — |
| rs3122703 | 9:15,608,986 | A/T | — | — |
| rs3122702 | 9:15,609,961 | T/A | — | — |
| rs6474931 | 9:15,617,677 | G/T | intron variant | — |
| rs765682018 | 9:15,623,268 | C/A | — | uncertain significance |
| rs2539727109 | 9:15,623,298 | A/G | — | uncertain significance |
| rs754692204 | 9:15,623,307 | A/C | — | uncertain significance |
| rs200870154 | 9:15,623,338 | A/T | — | uncertain significance |
| rs6474933 | 9:15,623,475 | A/C | — | — |
| rs4740619 | 9:15,634,326 | T/A | — | — |
| rs7042475 | 9:15,642,883 | A/G | intron variant | — |
| rs9776097 | 9:15,647,348 | G/T | intron variant | — |
| rs6474945 | 9:15,670,492 | G/C | — | — |
| rs138368957 | 9:15,678,788 | A/C | — | uncertain significance |
| rs370605119 | 9:15,678,805 | G/A | — | uncertain significance |
| rs543500235 | 9:15,678,816 | G/T | — | uncertain significance |
| rs370235683 | 9:15,678,820 | G/A | — | uncertain significance |
| rs560190847 | 9:15,678,850 | T/C | — | uncertain significance |
| rs777107054 | 9:15,678,851 | A/G | — | uncertain significance |
| rs10122339 | 9:15,691,712 | G/T | intron variant | — |
| rs771672077 | 9:15,695,233 | G/T | — | uncertain significance |
| rs200536745 | 9:15,695,245 | C/G | — | uncertain significance |
| rs2051129445 | 9:15,695,281 | A/G | — | uncertain significance |
| rs368291392 | 9:15,721,778 | G/C | — | uncertain significance |
| rs773274061 | 9:15,721,797 | G/C | — | uncertain significance |
| rs763283023 | 9:15,721,827 | G/A | — | uncertain significance |
| rs369675226 | 9:15,721,851 | A/T | — | uncertain significance |
| rs75279374 | 9:15,723,682 | A/C | — | benign |
| rs773212402 | 9:15,723,706 | A/C | — | uncertain significance |
| rs113840314 | 9:15,724,776 | A/T | — | likely benign |
| rs2537557788 | 9:15,724,861 | T/A | — | uncertain significance |
| rs200459237 | 9:15,724,882 | G/A | — | uncertain significance |
| rs750444306 | 9:15,724,925 | C/G | — | uncertain significance |
| rs371886499 | 9:15,724,945 | C/T | — | uncertain significance |
| rs149211044 | 9:15,727,916 | G/T | — | uncertain significance |
| rs760511140 | 9:15,727,973 | G/A | — | uncertain significance |
| rs756481660 | 9:15,728,011 | G/C | — | uncertain significance |
| rs775179144 | 9:15,728,018 | A/G | — | uncertain significance |
| rs748175444 | 9:15,728,026 | A/G | — | uncertain significance |
| rs1388455654 | 9:15,729,616 | T/A | — | uncertain significance |
| rs766371133 | 9:15,729,620 | G/C | — | uncertain significance |
| rs2537654655 | 9:15,729,753 | T/A | — | uncertain significance |
| rs531198274 | 9:15,744,280 | G/A | — | uncertain significance |
| rs377313812 | 9:15,744,316 | A/G | — | uncertain significance |
| rs1449557777 | 9:15,744,396 | G/A | — | uncertain significance |
| rs781713661 | 9:15,744,499 | A/T | — | uncertain significance |
| rs147702342 | 9:15,744,616 | C/T | — | uncertain significance |
| rs772838312 | 9:15,744,617 | G/A | — | uncertain significance |
| rs193920965 | 9:15,744,625 | C/T | — | uncertain significance |
| rs79919960 | 9:15,744,642 | T/A | — | benign |
| rs2537922115 | 9:15,744,662 | T/C | — | uncertain significance |
| rs149008818 | 9:15,744,758 | A/G | — | uncertain significance |
| rs544298455 | 9:15,745,546 | C/T | — | uncertain significance |
| rs778515156 | 9:15,745,557 | C/G | — | uncertain significance |
| rs747672518 | 9:15,745,558 | T/C | — | uncertain significance |
| rs376907295 | 9:15,745,569 | G/T | — | uncertain significance |
| rs568264542 | 9:15,745,614 | G/A | — | uncertain significance |
| rs910544807 | 9:15,745,621 | G/C | — | uncertain significance |
| rs772588407 | 9:15,777,622 | A/G | — | uncertain significance |
| rs201932972 | 9:15,777,640 | C/G | — | uncertain significance |
| rs554764647 | 9:15,777,714 | A/G | — | uncertain significance |
| rs753052796 | 9:15,777,736 | A/G | — | uncertain significance |
| rs141258483 | 9:15,777,823 | C/T | — | likely benign |
| rs139178402 | 9:15,778,989 | G/C | — | uncertain significance |
| rs369866643 | 9:15,779,005 | A/G | — | uncertain significance |
| rs373132680 | 9:15,779,038 | C/T | — | uncertain significance |
| rs769396946 | 9:15,779,055 | G/C | — | uncertain significance |
| rs374296923 | 9:15,779,144 | A/G | — | uncertain significance |
| rs2057837191 | 9:15,784,541 | G/T | — | uncertain significance |
| rs750226400 | 9:15,784,568 | G/A | — | uncertain significance |
| rs2538620733 | 9:15,784,586 | T/A | — | uncertain significance |
| rs142381025 | 9:15,784,603 | G/A | — | uncertain significance |
| rs535284505 | 9:15,784,671 | A/C | — | uncertain significance |
| rs9650685 | 9:15,808,994 | T/A | intron variant | — |
| rs2539630437 | 9:15,846,707 | C/T | — | uncertain significance |
| rs762751151 | 9:15,846,740 | A/C | — | uncertain significance |
| rs374545016 | 9:15,846,749 | G/A | — | uncertain significance |
| rs2539631792 | 9:15,846,762 | A/T | — | uncertain significance |
| rs1055103279 | 9:15,846,823 | A/G | — | uncertain significance |
Showing 100 of 123 variants. Use the SNP search for the full list.
Gene information from NCBI Gene. Variant classifications from ClinVar.