ZNF318

zinc finger protein 318

Summary

Predicted to enable protein heterodimerization activity and protein homodimerization activity. Predicted to be involved in negative regulation of DNA-templated transcription and positive regulation of DNA-templated transcription. Located in cytosol and nucleoplasm. [provided by Alliance of Genome Resources, Jul 2025]

Known Variants138 total

rsid	Position (GRCh37)	Alleles	Class	ClinVar
rs200855758	6:43,304,912	G/C	—	uncertain significance
rs753417070	6:43,304,934	C/T	—	uncertain significance
rs757598093	6:43,304,946	T/C	—	likely benign
rs2534263996	6:43,304,969	G/A	—	uncertain significance
rs1196809186	6:43,304,972	A/G	—	uncertain significance
rs753498583	6:43,305,015	A/C	—	uncertain significance
rs200489854	6:43,305,018	C/G	—	uncertain significance
rs752028362	6:43,305,023	G/T	—	uncertain significance
rs768825837	6:43,305,045	C/T	—	likely benign
rs368231307	6:43,305,062	A/C	—	uncertain significance
rs151125945	6:43,305,068	A/G	—	likely benign
rs749263212	6:43,305,083	G/T	—	uncertain significance
rs139964158	6:43,305,097	C/T	—	likely benign
rs190813585	6:43,305,285	G/C	—	uncertain significance
rs1332083888	6:43,305,449	C/A	—	uncertain significance
rs529917320	6:43,305,546	G/T	—	uncertain significance
rs750566293	6:43,305,558	C/T	—	likely benign
rs147972979	6:43,305,565	G/A	—	likely benign
rs778887279	6:43,305,578	C/T	—	uncertain significance
rs1178898928	6:43,305,591	C/T	—	uncertain significance
rs1779308928	6:43,305,600	C/T	—	uncertain significance
rs372980523	6:43,305,654	G/A	—	uncertain significance
rs34761878	6:43,305,790	T/C	—	benign
rs142925461	6:43,305,832	G/C	—	likely benign
rs199654348	6:43,305,912	T/C	—	uncertain significance
rs2534266094	6:43,305,929	C/G	—	uncertain significance
rs371578072	6:43,305,970	C/A	—	uncertain significance
rs1352012797	6:43,306,026	A/C	—	uncertain significance
rs778199866	6:43,306,032	T/C	—	likely benign
rs1235824206	6:43,306,073	G/C	—	uncertain significance
rs772707453	6:43,306,088	G/C	—	uncertain significance
rs375413097	6:43,306,282	C/A	—	uncertain significance
rs768078209	6:43,306,316	T/A	—	uncertain significance
rs2534267049	6:43,306,401	T/C	—	uncertain significance
rs369701277	6:43,306,423	T/G	—	uncertain significance
rs777116491	6:43,306,430	T/A	—	uncertain significance
rs574684582	6:43,306,485	G/A	—	uncertain significance
rs571927007	6:43,306,598	G/A	—	uncertain significance
rs149020638	6:43,306,625	A/T	—	uncertain significance
rs113147071	6:43,306,678	A/G	—	likely benign
rs772177873	6:43,306,748	C/T	—	likely benign
rs776342191	6:43,306,818	T/A	—	uncertain significance
rs751249218	6:43,306,893	T/C	—	uncertain significance
rs566380809	6:43,306,901	G/A	—	uncertain significance
rs1476201548	6:43,306,913	T/C	—	uncertain significance
rs151153042	6:43,307,092	C/T	—	benign
rs200065307	6:43,307,255	T/C	—	uncertain significance
rs774742513	6:43,307,265	C/T	—	uncertain significance
rs200747117	6:43,307,322	T/C	—	likely benign
rs2534268626	6:43,307,357	T/G	—	uncertain significance
rs145629243	6:43,307,399	G/A	—	benign
rs779769930	6:43,307,417	A/G	—	uncertain significance
rs771236798	6:43,307,433	G/A	—	uncertain significance
rs754565748	6:43,307,582	G/A	—	uncertain significance
rs931806707	6:43,307,583	T/C	—	uncertain significance
rs752092673	6:43,307,789	T/G	—	uncertain significance
rs143146213	6:43,307,837	A/T	—	uncertain significance
rs200041436	6:43,308,030	G/C	—	uncertain significance
rs1232515497	6:43,308,088	C/G	—	uncertain significance
rs1484812591	6:43,308,095	T/C	—	uncertain significance
rs182624602	6:43,308,191	C/T	—	uncertain significance
rs2534270614	6:43,308,641	C/G	—	uncertain significance
rs757137064	6:43,309,880	G/A	—	uncertain significance
rs143315352	6:43,309,888	G/T	—	uncertain significance
rs761694610	6:43,310,531	C/A	—	uncertain significance
rs1581640197	6:43,310,555	C/A	—	uncertain significance
rs778365453	6:43,310,574	T/C	—	uncertain significance
rs376986876	6:43,316,066	T/C	—	uncertain significance
rs2480899475	6:43,316,306	A/G	—	uncertain significance
rs776421567	6:43,316,356	C/T	—	uncertain significance
rs779662674	6:43,320,132	C/T	—	uncertain significance
rs777041821	6:43,320,162	T/A	—	uncertain significance
rs2480905904	6:43,320,208	C/T	—	uncertain significance
rs1725163651	6:43,322,426	C/A	—	uncertain significance
rs746542786	6:43,322,440	T/C	—	uncertain significance
rs2480909616	6:43,322,494	G/C	—	uncertain significance
rs777503911	6:43,322,496	G/A	—	uncertain significance
rs374413744	6:43,322,499	G/A	—	uncertain significance
rs749961788	6:43,322,598	G/C	—	uncertain significance
rs201794168	6:43,322,602	T/C	—	likely benign
rs976171019	6:43,322,665	G/A	—	uncertain significance
rs946207889	6:43,322,704	C/T	—	uncertain significance
rs758697100	6:43,322,713	A/T	—	uncertain significance
rs200407364	6:43,322,757	G/A	—	uncertain significance
rs370649269	6:43,322,792	C/A	—	uncertain significance
rs529534741	6:43,322,814	G/T	—	uncertain significance
rs1187640085	6:43,322,836	G/A	—	uncertain significance
rs768685421	6:43,322,883	C/G	—	uncertain significance
rs143830243	6:43,322,907	A/G	—	uncertain significance
rs1049243931	6:43,322,988	T/C	—	uncertain significance
rs2480910797	6:43,323,013	G/A	—	uncertain significance
rs201877430	6:43,323,105	C/T	—	uncertain significance
rs561784165	6:43,323,152	A/G	—	likely benign
rs200379733	6:43,323,156	T/C	—	uncertain significance
rs199685177	6:43,323,174	C/T	—	uncertain significance
rs1779593955	6:43,323,248	A/C	—	uncertain significance
rs368475526	6:43,323,277	T/C	—	uncertain significance
rs1779595793	6:43,323,348	G/A	—	uncertain significance
rs142200259	6:43,323,465	T/C	—	uncertain significance
rs2480912228	6:43,323,492	C/T	—	uncertain significance

Showing 100 of 138 variants. Use the SNP search for the full list.

Gene information from NCBI Gene. Variant classifications from ClinVar.