ZNF646

zinc finger protein 646

Summary

Predicted to enable DNA-binding transcription factor activity, RNA polymerase II-specific and RNA polymerase II cis-regulatory region sequence-specific DNA binding activity. Predicted to be involved in regulation of DNA-templated transcription. Predicted to be located in nucleus. [provided by Alliance of Genome Resources, Jul 2025]

Known Variants145 total

rsid	Position (GRCh37)	Alleles	Class	ClinVar
rs11642192	16:31,082,025	T/C	upstream gene variant	—
rs7197717	16:31,083,075	A/T	—	—
rs150512037	16:31,087,688	C/T	—	uncertain significance
rs1039884198	16:31,087,689	G/A	—	uncertain significance
rs139437413	16:31,087,719	G/A	—	uncertain significance
rs2544048485	16:31,087,752	A/G	—	uncertain significance
rs1043699461	16:31,087,757	A/G	—	uncertain significance
rs755048148	16:31,087,845	G/T	—	uncertain significance
rs765730146	16:31,087,899	C/G	—	uncertain significance
rs199961738	16:31,087,940	C/T	—	uncertain significance
rs760178081	16:31,087,952	C/T	—	uncertain significance
rs1024018257	16:31,087,965	C/T	—	uncertain significance
rs1303912541	16:31,087,977	A/G	—	uncertain significance
rs375213551	16:31,088,007	C/T	—	uncertain significance
rs369533379	16:31,088,069	A/G	—	uncertain significance
rs1567405814	16:31,088,076	C/A	—	uncertain significance
rs1224265852	16:31,088,216	A/G	—	uncertain significance
rs200365125	16:31,088,333	T/G	—	uncertain significance
rs749671	16:31,088,347	G/C	missense variant	—
rs770793139	16:31,088,534	C/G	—	uncertain significance
rs373725273	16:31,088,546	C/T	—	uncertain significance
rs749670	16:31,088,625	A/G	missense variant	—
rs1274440751	16:31,088,664	G/C	—	uncertain significance
rs199698997	16:31,088,695	G/A	—	uncertain significance
rs2544055406	16:31,088,715	T/G	—	uncertain significance
rs1008075548	16:31,088,759	C/T	—	uncertain significance
rs775251138	16:31,088,768	C/T	—	uncertain significance
rs757118528	16:31,088,927	C/A	—	uncertain significance
rs147030622	16:31,088,931	G/C	—	uncertain significance
rs778897604	16:31,089,026	G/A	—	uncertain significance
rs779510574	16:31,089,141	G/A	—	uncertain significance
rs1042034030	16:31,089,153	A/G	—	uncertain significance
rs1241671184	16:31,089,159	T/C	—	uncertain significance
rs771377440	16:31,089,179	C/T	—	uncertain significance
rs775558415	16:31,089,201	G/A	—	uncertain significance
rs146467604	16:31,089,206	A/G	—	uncertain significance
rs550523509	16:31,089,239	C/T	—	uncertain significance
rs752141159	16:31,089,258	C/T	—	uncertain significance
rs2544058478	16:31,089,261	C/T	—	uncertain significance
rs568763528	16:31,089,267	C/G	—	uncertain significance
rs371616266	16:31,089,419	C/T	—	uncertain significance
rs1190107304	16:31,089,486	C/G	—	uncertain significance
rs760483920	16:31,089,504	G/A	—	uncertain significance
rs760164180	16:31,089,524	C/T	—	uncertain significance
rs2057103673	16:31,089,530	T/G	—	uncertain significance
rs72785532	16:31,089,532	A/T	—	likely benign
rs768404020	16:31,089,605	C/T	—	uncertain significance
rs772812471	16:31,089,635	C/T	—	uncertain significance
rs142395653	16:31,089,636	G/A	—	uncertain significance
rs764412425	16:31,089,648	G/A	—	uncertain significance
rs75918054	16:31,089,651	G/A	—	uncertain significance
rs368619168	16:31,089,653	C/T	—	uncertain significance
rs147667959	16:31,089,663	G/A	—	uncertain significance
rs769524805	16:31,089,675	G/A	—	uncertain significance
rs1173660350	16:31,089,704	G/A	—	uncertain significance
rs371062492	16:31,089,720	C/T	—	uncertain significance
rs758461491	16:31,089,724	G/C	—	uncertain significance
rs781216621	16:31,089,734	C/T	—	uncertain significance
rs770530563	16:31,089,750	A/G	—	likely benign
rs746959210	16:31,089,816	A/G	—	uncertain significance
rs995203377	16:31,089,827	G/T	—	uncertain significance
rs200858016	16:31,089,834	T/C	—	uncertain significance
rs375424774	16:31,089,852	G/A	—	uncertain significance
rs867866760	16:31,089,918	G/T	—	uncertain significance
rs753628879	16:31,089,981	G/A	—	uncertain significance
rs1169784907	16:31,089,999	G/A	—	uncertain significance
rs749589689	16:31,090,053	A/G	—	likely benign
rs566216572	16:31,090,074	A/G	—	uncertain significance
rs775659079	16:31,090,079	G/C	—	uncertain significance
rs781579333	16:31,090,344	G/A	—	uncertain significance
rs757373121	16:31,090,430	C/G	—	uncertain significance
rs377644012	16:31,090,431	G/A	—	likely benign
rs2544066018	16:31,090,467	T/C	—	uncertain significance
rs370941195	16:31,090,481	C/T	—	uncertain significance
rs151285758	16:31,090,482	G/A	—	uncertain significance
rs370961838	16:31,090,550	G/A	—	uncertain significance
rs201429296	16:31,090,643	A/G	—	uncertain significance
rs776128371	16:31,090,695	G/T	—	uncertain significance
rs368754362	16:31,090,713	A/C	—	uncertain significance
rs371911144	16:31,090,788	A/T	—	uncertain significance
rs375247820	16:31,090,971	C/T	—	uncertain significance
rs201284147	16:31,091,059	C/G	—	uncertain significance
rs751103542	16:31,091,189	A/C	—	uncertain significance
rs1300637758	16:31,091,246	C/T	—	uncertain significance
rs62057086	16:31,091,314	G/C	—	uncertain significance
rs35376811	16:31,091,390	C/T	—	likely benign
rs766704859	16:31,091,391	G/A	—	uncertain significance
rs140878497	16:31,091,421	G/A	—	uncertain significance
rs749277221	16:31,091,486	A/G	—	uncertain significance
rs150156564	16:31,091,495	C/T	—	uncertain significance
rs368825645	16:31,091,513	C/G	—	uncertain significance
rs200908817	16:31,091,514	G/C	—	uncertain significance
rs771282048	16:31,091,558	G/A	—	uncertain significance
rs775744443	16:31,091,570	C/T	—	uncertain significance
rs761941293	16:31,091,579	G/A	—	uncertain significance
rs758106451	16:31,091,597	C/T	—	uncertain significance
rs374257528	16:31,091,609	G/A	—	uncertain significance
rs1279119320	16:31,091,610	A/G	—	uncertain significance
rs955871060	16:31,091,620	G/C	—	uncertain significance
rs762906939	16:31,091,657	C/T	—	uncertain significance

Showing 100 of 145 variants. Use the SNP search for the full list.

Gene information from NCBI Gene. Variant classifications from ClinVar.