ZCCHC2

zinc finger CCHC-type containing 2

Summary

Predicted to enable nucleic acid binding activity; phosphatidylinositol binding activity; and zinc ion binding activity. Located in cytoplasm. [provided by Alliance of Genome Resources, Jul 2025]

Known Variants96 total

rsid	Position (GRCh37)	Alleles	Class	ClinVar
rs962440736	18:60,190,688	A/G	—	uncertain significance
rs751177226	18:60,190,694	C/G	—	uncertain significance
rs745842831	18:60,190,704	C/T	—	uncertain significance
rs769612317	18:60,190,706	C/T	—	uncertain significance
rs1303933394	18:60,190,724	C/T	—	uncertain significance
rs749046042	18:60,190,730	G/T	—	likely benign
rs2511673466	18:60,190,735	C/G	—	uncertain significance
rs1015613321	18:60,190,749	C/T	—	uncertain significance
rs1914151545	18:60,190,751	A/G	—	uncertain significance
rs1914151788	18:60,190,752	A/C	—	uncertain significance
rs1914153096	18:60,190,760	T/C	—	uncertain significance
rs1469731804	18:60,190,814	C/T	—	uncertain significance
rs927746382	18:60,190,827	C/T	—	uncertain significance
rs915021992	18:60,190,833	C/G	—	likely benign
rs1914170080	18:60,190,848	C/T	—	uncertain significance
rs1882224170	18:60,190,851	G/A	—	uncertain significance
rs934876005	18:60,190,868	G/A	—	uncertain significance
rs1441172295	18:60,190,880	G/C	—	uncertain significance
rs563696641	18:60,190,881	C/G	—	likely benign
rs773598526	18:60,190,917	G/C	—	uncertain significance
rs2511673980	18:60,190,932	T/C	—	uncertain significance
rs753184953	18:60,191,020	G/C	—	likely benign
rs2511674151	18:60,191,033	G/A	—	uncertain significance
rs944419631	18:60,191,063	G/T	—	uncertain significance
rs558674770	18:60,191,105	G/A	—	uncertain significance
rs1420315502	18:60,191,159	G/A	—	uncertain significance
rs1358970465	18:60,191,211	G/C	—	uncertain significance
rs2511675089	18:60,191,417	A/G	—	uncertain significance
rs911427230	18:60,191,454	C/G	—	uncertain significance
rs1041585800	18:60,191,479	C/A	—	uncertain significance
rs746057971	18:60,191,576	T/G	—	uncertain significance
rs35331358	18:60,203,140	C/A	intron variant	—
rs17070072	18:60,205,542	T/G	intron variant	—
rs55722786	18:60,206,800	G/T	intron variant	—
rs182227591	18:60,206,924	C/T	—	uncertain significance
rs373430765	18:60,206,927	A/G	—	uncertain significance
rs748604052	18:60,206,940	G/A	—	uncertain significance
rs201863625	18:60,206,951	A/G	—	uncertain significance
rs199538253	18:60,206,965	G/A	—	uncertain significance
rs142239484	18:60,207,797	T/A	intron variant	—
rs747426951	18:60,209,739	A/G	—	uncertain significance
rs867259093	18:60,209,753	G/A	—	uncertain significance
rs2145498243	18:60,209,772	A/C	—	uncertain significance
rs761095748	18:60,209,781	G/A	—	uncertain significance
rs369581993	18:60,217,666	G/A	—	uncertain significance
rs12172847	18:60,223,017	G/T	—	—
rs2048793	18:60,224,279	T/G	—	—
rs892899746	18:60,225,935	C/T	—	uncertain significance
rs778171889	18:60,227,847	A/G	—	uncertain significance
rs376877137	18:60,230,312	G/A	—	uncertain significance
rs2511706456	18:60,230,323	G/C	—	uncertain significance
rs374587965	18:60,230,343	A/G	—	uncertain significance
rs550649336	18:60,230,366	T/C	—	uncertain significance
rs1237303537	18:60,231,823	G/A	—	uncertain significance
rs746716197	18:60,231,825	T/G	—	uncertain significance
rs1278468184	18:60,231,845	G/C	—	uncertain significance
rs61740184	18:60,232,248	A/G	—	likely benign
rs928705945	18:60,232,282	G/A	—	uncertain significance
rs1227807386	18:60,232,290	C/G	—	uncertain significance
rs375909728	18:60,232,293	T/C	—	uncertain significance
rs2511708222	18:60,232,322	T/C	—	likely benign
rs781659795	18:60,237,360	G/T	—	uncertain significance
rs1417384728	18:60,237,404	C/T	—	uncertain significance
rs200296776	18:60,237,405	C/T	missense variant	—
rs772233346	18:60,241,349	G/A	—	uncertain significance
rs763625292	18:60,241,401	T/G	—	uncertain significance
rs367680462	18:60,241,427	G/A	—	uncertain significance
rs1916709440	18:60,241,490	A/G	—	uncertain significance
rs747142530	18:60,241,541	G/A	—	likely benign
rs532980655	18:60,241,580	G/A	—	uncertain significance
rs761412542	18:60,241,603	G/T	—	uncertain significance
rs201968749	18:60,241,617	C/T	—	likely benign
rs541209798	18:60,241,649	A/C	—	uncertain significance
rs199663644	18:60,241,659	C/T	—	uncertain significance
rs767666189	18:60,241,733	G/T	—	uncertain significance
rs746550438	18:60,241,785	C/G	—	uncertain significance
rs2511715301	18:60,241,869	A/G	—	uncertain significance
rs762756414	18:60,241,908	C/T	—	uncertain significance
rs2511715371	18:60,241,928	G/C	—	uncertain significance
rs200293690	18:60,241,929	C/A	—	uncertain significance
rs574841597	18:60,241,940	G/C	—	uncertain significance
rs768507813	18:60,242,013	T/C	—	uncertain significance
rs774124434	18:60,242,027	G/T	—	uncertain significance
rs763058669	18:60,242,141	C/T	—	uncertain significance
rs373412830	18:60,242,303	G/A	—	uncertain significance
rs191537238	18:60,242,337	G/T	—	uncertain significance
rs918510081	18:60,242,345	C/T	—	uncertain significance
rs2511716402	18:60,242,358	G/T	—	uncertain significance
rs199658152	18:60,242,428	G/A	—	uncertain significance
rs765522998	18:60,242,483	G/A	—	uncertain significance
rs767900360	18:60,242,615	A/G	—	uncertain significance
rs2511717000	18:60,242,675	A/G	—	uncertain significance
rs747772285	18:60,242,775	A/G	—	likely benign
rs1429847131	18:60,243,756	C/G	—	uncertain significance
rs745813308	18:60,243,780	C/A	—	uncertain significance
rs775275680	18:60,243,787	A/T	—	uncertain significance

Gene information from NCBI Gene. Variant classifications from ClinVar.