TNRC18

trinucleotide repeat containing 18

Summary

Predicted to enable chromatin binding activity. Located in cytosol; mitochondrion; and nucleus. [provided by Alliance of Genome Resources, Jul 2025]

Known Variants463 total

rsid	Position (GRCh37)	Alleles	Class	ClinVar
rs755613149	7:5,347,741	C/T	—	uncertain significance
rs62441157	7:5,347,746	C/T	—	benign
rs9639976	7:5,347,749	A/G	—	benign
rs1270292355	7:5,347,790	C/T	—	uncertain significance
rs370539555	7:5,347,827	C/G	—	uncertain significance
rs202187831	7:5,347,860	C/T	—	likely benign
rs11554710	7:5,347,914	A/G	—	benign
rs532939555	7:5,347,948	G/A	—	likely benign
rs746360360	7:5,348,482	A/C	—	benign
rs560820937	7:5,348,503	T/G	—	likely benign
rs1446406439	7:5,348,524	C/G	—	uncertain significance
rs750268247	7:5,348,537	C/T	—	uncertain significance
rs528373278	7:5,348,546	G/A	—	uncertain significance
rs1277953751	7:5,348,552	A/C	—	uncertain significance
rs186045924	7:5,348,725	G/A	—	benign
rs199955791	7:5,348,767	C/T	—	likely benign
rs760948933	7:5,348,772	G/T	—	uncertain significance
rs141271017	7:5,348,784	G/C	—	benign
rs374119604	7:5,348,787	C/T	—	likely benign
rs2546519528	7:5,348,801	C/G	—	uncertain significance
rs183471188	7:5,348,811	G/A	—	benign
rs367586045	7:5,348,869	C/T	—	uncertain significance
rs2546520333	7:5,348,936	T/C	—	uncertain significance
rs1227492053	7:5,348,947	C/T	—	uncertain significance
rs749942884	7:5,348,961	G/A	—	likely benign
rs1483654551	7:5,348,969	G/T	—	uncertain significance
rs1787336094	7:5,352,184	C/T	—	uncertain significance
rs374974528	7:5,352,259	C/T	—	uncertain significance
rs752847334	7:5,352,282	C/T	—	uncertain significance
rs1183121106	7:5,352,375	G/A	—	uncertain significance
rs780459767	7:5,352,390	C/T	—	uncertain significance
rs534653312	7:5,352,393	G/A	—	uncertain significance
rs181237498	7:5,352,403	C/T	—	benign
rs577991475	7:5,352,439	C/A	—	conflicting classifications of pathogenicity
rs768840123	7:5,352,450	G/A	—	uncertain significance
rs774616116	7:5,352,451	C/T	—	uncertain significance
rs767803377	7:5,352,453	G/A	—	uncertain significance
rs1306379608	7:5,352,475	C/T	—	uncertain significance
rs369628537	7:5,352,489	G/T	—	uncertain significance
rs745794619	7:5,352,500	G/C	—	uncertain significance
rs116600716	7:5,352,512	G/A	—	benign
rs376153797	7:5,352,530	G/A	—	likely benign
rs760867022	7:5,352,540	G/A	—	uncertain significance
rs753212093	7:5,352,552	G/A	—	uncertain significance
rs939081403	7:5,352,554	C/A	—	likely benign
rs757833275	7:5,352,564	G/A	—	uncertain significance
rs777331564	7:5,352,567	G/A	—	uncertain significance
rs191091261	7:5,352,587	C/T	—	likely benign
rs780070335	7:5,352,620	G/T	—	likely benign
rs891390068	7:5,352,635	T/G	—	likely benign
rs112435102	7:5,352,650	G/T	—	likely benign
rs778943778	7:5,352,656	G/T	—	likely benign
rs138591330	7:5,352,659	G/T	—	benign
rs866165739	7:5,352,665	T/G	—	likely benign
rs1022523938	7:5,352,682	A/C	—	uncertain significance
rs763417600	7:5,352,694	C/T	—	uncertain significance
rs114222264	7:5,352,731	G/A	—	benign
rs1583727477	7:5,352,733	T/C	—	likely benign
rs186451318	7:5,352,737	G/A	—	benign
rs1264904511	7:5,352,790	C/T	—	likely benign
rs191028877	7:5,352,791	G/A	—	likely benign
rs1044262868	7:5,352,793	T/C	—	uncertain significance
rs772892260	7:5,352,835	T/C	—	uncertain significance
rs183183335	7:5,352,860	G/C	—	benign
rs2546542679	7:5,352,871	G/C	—	uncertain significance
rs1461548043	7:5,352,891	G/A	—	uncertain significance
rs990583844	7:5,352,902	G/T	—	uncertain significance
rs538690867	7:5,352,938	C/A	—	conflicting classifications of pathogenicity
rs76882791	7:5,352,949	G/C	—	benign
rs759287371	7:5,352,956	G/A	—	likely benign
rs553478741	7:5,352,964	C/T	—	uncertain significance
rs571803048	7:5,352,998	G/A	—	likely benign
rs541115382	7:5,353,002	G/A	—	uncertain significance
rs1364885416	7:5,353,006	G/T	—	uncertain significance
rs753919497	7:5,353,009	G/A	—	uncertain significance
rs932227705	7:5,353,036	T/C	—	uncertain significance
rs761630802	7:5,353,037	G/C	—	likely benign
rs371177133	7:5,353,055	C/T	—	likely benign
rs188607046	7:5,353,061	C/T	—	benign
rs748908543	7:5,353,072	G/A	—	uncertain significance
rs530723738	7:5,353,086	T/G	—	uncertain significance
rs201969561	7:5,353,136	G/A	—	likely benign
rs560747034	7:5,353,147	C/T	—	uncertain significance
rs199863123	7:5,353,161	G/A	—	uncertain significance
rs776731384	7:5,353,174	C/A	—	uncertain significance
rs201143658	7:5,353,222	G/A	—	uncertain significance
rs781209483	7:5,353,231	G/A	—	uncertain significance
rs58819185	7:5,353,252	G/C	—	benign
rs140781391	7:5,353,253	G/T	—	benign
rs765681757	7:5,353,342	G/A	—	uncertain significance
rs12532973	7:5,353,344	A/G	—	benign
rs767310790	7:5,353,350	G/A	—	uncertain significance
rs534146863	7:5,353,353	C/A	—	uncertain significance
rs771097631	7:5,353,359	T/C	—	uncertain significance
rs2546546292	7:5,353,381	C/A	—	uncertain significance
rs1787550925	7:5,353,383	A/G	—	uncertain significance
rs773873114	7:5,353,403	C/G	—	uncertain significance
rs760544399	7:5,353,411	C/G	—	uncertain significance
rs1335171101	7:5,353,419	C/G	—	uncertain significance
rs753700845	7:5,353,423	T/C	—	uncertain significance

Showing 100 of 463 variants. Use the SNP search for the full list.

Gene information from NCBI Gene. Variant classifications from ClinVar.