CCDC178

coiled-coil domain containing 178

Summary

Located in ciliary basal body. [provided by Alliance of Genome Resources, Jul 2025]

Known Variants67 total

rsid	Position (GRCh37)	Alleles	Class	ClinVar
rs200567065	18:30,517,983	C/T	—	uncertain significance
rs1440559611	18:30,518,028	T/C	—	uncertain significance
rs17739703	18:30,523,288	T/C	intron variant	—
rs201959675	18:30,554,575	T/C	—	uncertain significance
rs7234969	18:30,590,177	C/T	regulatory region variant	—
rs77363699	18:30,626,497	T/A	intron variant	—
rs405575	18:30,665,343	C/T	intron variant	—
rs368292012	18:30,672,742	T/C	—	likely benign
rs186514123	18:30,672,771	T/C	—	uncertain significance
rs2511370278	18:30,672,793	T/G	—	uncertain significance
rs368493349	18:30,672,825	T/C	—	uncertain significance
rs62090751	18:30,672,840	C/A	—	likely benign
rs271581	18:30,713,247	A/T	intron variant	—
rs271582	18:30,714,148	T/C	intron variant	—
rs271584	18:30,717,321	G/A	—	—
rs271526	18:30,776,791	G/T	intron variant	—
rs528805719	18:30,791,916	C/T	—	uncertain significance
rs2511560637	18:30,791,976	T/C	—	likely benign
rs927384416	18:30,794,388	A/C	—	—
rs761771379	18:30,795,553	T/C	—	uncertain significance
rs767429656	18:30,795,554	C/T	—	likely benign
rs760474921	18:30,795,560	T/C	—	uncertain significance
rs576629806	18:30,795,622	G/C	—	uncertain significance
rs141556619	18:30,795,623	T/C	—	likely benign
rs2511568717	18:30,795,650	A/G	—	uncertain significance
rs150710440	18:30,795,653	G/A	—	uncertain significance
rs752191887	18:30,795,658	C/T	—	uncertain significance
rs201497010	18:30,803,075	T/A	—	uncertain significance
rs182556774	18:30,803,117	A/T	—	uncertain significance
rs763554535	18:30,803,124	C/A	—	uncertain significance
rs147051362	18:30,803,132	T/C	—	uncertain significance
rs564793450	18:30,804,755	T/C	—	uncertain significance
rs1433024006	18:30,804,768	T/C	—	uncertain significance
rs771437193	18:30,804,801	G/A	—	uncertain significance
rs144365664	18:30,804,839	C/G	—	uncertain significance
rs763456731	18:30,804,870	C/T	—	uncertain significance
rs771619759	18:30,804,890	T/C	—	uncertain significance
rs117054944	18:30,825,215	C/T	—	likely benign
rs371328695	18:30,825,258	T/C	—	uncertain significance
rs140513669	18:30,825,291	C/T	—	uncertain significance
rs2510870411	18:30,825,368	T/A	—	uncertain significance
rs1051585747	18:30,825,385	T/C	—	uncertain significance
rs781169337	18:30,846,922	A/T	—	uncertain significance
rs371081933	18:30,846,940	G/A	—	likely benign
rs140707449	18:30,846,965	T/C	—	uncertain significance
rs373519668	18:30,847,001	T/C	—	uncertain significance
rs141705181	18:30,847,223	C/G	—	uncertain significance
rs768223876	18:30,873,137	A/T	—	uncertain significance
rs778271137	18:30,873,142	A/G	—	uncertain significance
rs759622933	18:30,873,182	T/G	—	uncertain significance
rs753584292	18:30,873,218	C/T	—	uncertain significance
rs1434676290	18:30,873,227	C/A	—	uncertain significance
rs549038999	18:30,873,235	G/A	—	uncertain significance
rs6507008	18:30,876,844	C/G	—	—
rs983599814	18:30,903,462	C/T	—	uncertain significance
rs199956098	18:30,903,467	A/G	—	uncertain significance
rs371866883	18:30,913,355	T/A	—	uncertain significance
rs528148899	18:30,926,181	G/T	—	uncertain significance
rs745408194	18:30,926,187	C/T	—	uncertain significance
rs6507016	18:30,927,775	C/T	intron variant	—
rs147462915	18:30,950,014	C/T	—	likely benign
rs749454417	18:30,950,114	C/T	—	uncertain significance
rs138740715	18:30,950,151	C/A	—	uncertain significance
rs150589600	18:30,969,593	C/T	—	likely benign
rs2511175774	18:30,977,167	T/C	—	uncertain significance
rs548517073	18:30,992,007	G/T	—	uncertain significance
rs6507022	18:30,998,131	G/C	intron variant	—

Gene information from NCBI Gene. Variant classifications from ClinVar.