IQCN

IQ motif containing N

Summary

Involved in spermatid development. Located in mitochondrion. Implicated in spermatogenic failure 78. [provided by Alliance of Genome Resources, Jul 2025]

Known Variants132 total

rsid	Position (GRCh37)	Alleles	Class	ClinVar
rs200030980	19:18,368,015	C/T	—	likely benign
rs200583656	19:18,368,051	G/A	—	uncertain significance
rs777166271	19:18,368,073	T/G	—	uncertain significance
rs139341013	19:18,368,117	G/A	—	uncertain significance
rs562355836	19:18,368,198	C/T	—	likely benign
rs139487168	19:18,368,201	T/C	—	likely benign
rs61740691	19:18,368,246	C/A	—	uncertain significance
rs144107214	19:18,368,313	G/A	—	uncertain significance
rs139912303	19:18,368,334	G/A	—	uncertain significance
rs748635735	19:18,368,369	G/A	—	uncertain significance
rs112108230	19:18,368,412	C/T	—	uncertain significance
rs761733054	19:18,368,438	C/T	—	uncertain significance
rs112806595	19:18,368,533	G/T	—	uncertain significance
rs147110090	19:18,368,552	C/T	—	likely benign
rs528994641	19:18,368,583	G/T	—	uncertain significance
rs548738319	19:18,368,603	G/A	—	uncertain significance
rs2512727907	19:18,368,606	G/T	—	uncertain significance
rs1302354266	19:18,368,633	C/T	—	uncertain significance
rs201837174	19:18,368,634	G/C	—	uncertain significance
rs777612220	19:18,368,637	G/A	—	uncertain significance
rs746725866	19:18,368,642	C/T	—	uncertain significance
rs143099659	19:18,368,643	G/A	—	likely benign
rs769410268	19:18,368,651	C/T	—	uncertain significance
rs375802609	19:18,368,706	G/A	—	uncertain significance
rs146173511	19:18,368,721	G/A	—	uncertain significance
rs61740685	19:18,368,748	C/T	—	uncertain significance
rs371327963	19:18,368,757	G/A	—	uncertain significance
rs759714402	19:18,368,787	T/C	—	likely benign
rs764350386	19:18,368,801	C/T	—	likely benign
rs145710367	19:18,368,828	C/A	—	uncertain significance
rs940767539	19:18,368,834	G/A	—	uncertain significance
rs2512728594	19:18,368,838	C/T	—	uncertain significance
rs764440191	19:18,368,871	C/T	—	uncertain significance
rs61740684	19:18,368,909	G/A	—	likely benign
rs1969494964	19:18,375,211	C/A	—	uncertain significance
rs1969495049	19:18,375,213	C/A	—	uncertain significance
rs765627790	19:18,375,256	C/A	—	uncertain significance
rs541324285	19:18,375,261	G/A	—	uncertain significance
rs1037275770	19:18,375,271	C/A	—	uncertain significance
rs371400971	19:18,375,291	G/A	—	uncertain significance
rs953333525	19:18,375,295	C/T	—	likely benign
rs754798274	19:18,375,320	C/T	—	likely benign
rs201716416	19:18,375,352	G/C	—	uncertain significance
rs368154814	19:18,375,450	A/G	—	uncertain significance
rs531854880	19:18,375,484	G/A	—	uncertain significance
rs371100161	19:18,375,510	C/T	—	uncertain significance
rs375229949	19:18,375,511	G/A	—	uncertain significance
rs758680967	19:18,375,554	C/T	—	uncertain significance
rs763428833	19:18,375,632	T/C	—	likely benign
rs2512737429	19:18,375,648	G/T	—	uncertain significance
rs766363898	19:18,375,739	C/A	—	uncertain significance
rs142351726	19:18,375,763	C/T	—	likely benign
rs148262698	19:18,375,784	G/C	—	uncertain significance
rs150764416	19:18,375,793	C/T	—	uncertain significance
rs775836909	19:18,375,814	C/T	—	uncertain significance
rs377401094	19:18,375,849	G/A	—	uncertain significance
rs772889466	19:18,375,891	C/G	—	uncertain significance
rs140540623	19:18,375,916	C/A	—	uncertain significance
rs757616379	19:18,375,918	T/C	—	uncertain significance
rs149314979	19:18,375,991	G/A	—	uncertain significance
rs780667666	19:18,376,005	T/C	—	uncertain significance
rs368056732	19:18,376,008	G/C	—	uncertain significance
rs373797917	19:18,376,020	C/T	—	uncertain significance
rs2512738999	19:18,376,066	C/G	—	uncertain significance
rs750849385	19:18,376,074	G/A	—	uncertain significance
rs779060634	19:18,376,105	T/C	—	likely benign
rs147485534	19:18,376,117	G/A	—	uncertain significance
rs761192366	19:18,376,125	G/A	—	uncertain significance
rs2512739467	19:18,376,218	G/T	—	uncertain significance
rs139682639	19:18,376,374	C/T	—	likely benign
rs572232343	19:18,376,375	G/A	—	uncertain significance
rs1301097479	19:18,376,426	C/T	—	uncertain significance
rs2512740162	19:18,376,470	T/A	—	uncertain significance
rs139728452	19:18,376,503	G/C	—	uncertain significance
rs2512740390	19:18,376,544	T/G	—	uncertain significance
rs751306707	19:18,376,572	G/C	—	uncertain significance
rs548364590	19:18,376,587	G/A	—	likely benign
rs753484620	19:18,376,602	A/T	—	uncertain significance
rs779264398	19:18,376,607	C/A	—	uncertain significance
rs151152365	19:18,376,629	T/C	—	likely benign
rs1969559661	19:18,376,654	C/G	—	uncertain significance
rs767407852	19:18,376,663	C/A	—	uncertain significance
rs138064943	19:18,376,745	C/T	—	likely benign
rs1969565264	19:18,376,756	G/A	—	uncertain significance
rs776515729	19:18,376,824	C/T	—	uncertain significance
rs1458385630	19:18,376,828	A/T	—	likely benign
rs764786631	19:18,376,848	A/G	—	uncertain significance
rs757676566	19:18,376,867	T/C	—	uncertain significance
rs1264767191	19:18,376,905	T/G	—	uncertain significance
rs1025196202	19:18,376,950	G/A	—	likely benign
rs2512741817	19:18,376,992	G/T	—	uncertain significance
rs1182788702	19:18,377,010	C/T	—	uncertain significance
rs559069767	19:18,377,013	G/A	—	uncertain significance
rs1040278321	19:18,377,053	G/C	—	uncertain significance
rs752703118	19:18,377,055	G/C	—	likely benign
rs139542395	19:18,377,103	C/T	—	uncertain significance
rs200263958	19:18,377,104	G/A	—	uncertain significance
rs570679686	19:18,377,116	T/G	—	uncertain significance
rs61740748	19:18,377,200	C/T	—	uncertain significance
rs752664961	19:18,377,277	G/A	—	uncertain significance

Showing 100 of 132 variants. Use the SNP search for the full list.

Gene information from NCBI Gene. Variant classifications from ClinVar.