NINL

ninein like

Summary

Predicted to enable calcium ion binding activity. Predicted to be involved in microtubule anchoring at centrosome. Located in centrosome. [provided by Alliance of Genome Resources, Jul 2025]

Known Variants106 total

rsid	Position (GRCh37)	Alleles	Class	ClinVar
rs1172991888	20:25,434,101	C/T	—	uncertain significance
rs753550459	20:25,434,110	C/A	—	uncertain significance
rs769227074	20:25,434,146	T/C	—	uncertain significance
rs2516099120	20:25,434,235	T/C	—	uncertain significance
rs6115189	20:25,434,254	G/T	—	uncertain significance
rs759262045	20:25,436,311	G/T	—	uncertain significance
rs949703317	20:25,439,075	G/A	—	uncertain significance
rs747375078	20:25,439,107	C/T	—	likely benign
rs372116474	20:25,439,108	G/A	—	uncertain significance
rs201845524	20:25,439,117	G/C	—	uncertain significance
rs116267316	20:25,439,125	T/C	—	likely benign
rs11087521	20:25,440,648	G/A	intron variant	—
rs139278158	20:25,442,190	G/C	—	likely benign
rs760945296	20:25,442,198	C/A	—	uncertain significance
rs2516229327	20:25,443,048	C/T	—	uncertain significance
rs140202244	20:25,443,081	G/A	—	uncertain significance
rs2062817577	20:25,443,172	C/G	—	uncertain significance
rs2062941385	20:25,448,021	T/A	—	uncertain significance
rs399899	20:25,449,858	G/A	—	—
rs11474838	20:25,449,887	T/G	intron variant	—
rs200797948	20:25,450,669	C/T	—	likely benign
rs182405752	20:25,450,678	C/T	—	uncertain significance
rs781608281	20:25,450,693	A/C	—	uncertain significance
rs746415148	20:25,450,696	A/G	—	uncertain significance
rs1021040275	20:25,450,711	G/C	—	uncertain significance
rs2063224000	20:25,456,690	T/G	—	uncertain significance
rs34225309	20:25,456,718	C/T	—	uncertain significance
rs563958229	20:25,456,887	C/T	—	uncertain significance
rs437635	20:25,456,888	A/G	—	benign
rs2063232177	20:25,456,890	T/C	—	likely benign
rs148788361	20:25,457,023	G/A	—	likely benign
rs751087888	20:25,457,138	G/A	—	uncertain significance
rs201894527	20:25,457,237	G/A	—	likely benign
rs770146727	20:25,457,247	C/T	—	uncertain significance
rs2063251034	20:25,457,253	C/A	—	uncertain significance
rs1213578090	20:25,457,258	C/T	—	uncertain significance
rs778029724	20:25,457,283	C/T	—	uncertain significance
rs781737602	20:25,457,291	C/A	—	uncertain significance
rs372683397	20:25,457,313	C/T	—	uncertain significance
rs1288491655	20:25,457,367	C/T	—	likely benign
rs199888621	20:25,457,375	G/A	—	likely benign
rs756698058	20:25,457,414	C/T	—	uncertain significance
rs374713970	20:25,457,439	G/T	—	uncertain significance
rs2516449199	20:25,457,442	G/C	—	uncertain significance
rs2516449451	20:25,457,449	C/G	—	uncertain significance
rs776699071	20:25,457,453	T/C	—	uncertain significance
rs762729377	20:25,457,469	G/A	—	uncertain significance
rs141954162	20:25,457,555	G/A	—	likely benign
rs780202897	20:25,457,583	C/A	—	uncertain significance
rs562974146	20:25,457,613	C/T	—	uncertain significance
rs370873099	20:25,457,678	G/A	—	uncertain significance
rs143118786	20:25,457,690	G/A	—	benign
rs192531829	20:25,459,586	C/T	—	uncertain significance
rs1375041987	20:25,459,674	G/A	—	uncertain significance
rs201963348	20:25,459,710	C/T	—	likely benign
rs760292434	20:25,459,743	C/T	—	uncertain significance
rs200310183	20:25,459,749	C/T	—	uncertain significance
rs368454403	20:25,459,767	G/A	—	uncertain significance
rs762323174	20:25,459,841	A/G	—	uncertain significance
rs767987874	20:25,459,842	C/A	—	uncertain significance
rs1215217505	20:25,460,845	C/G	—	uncertain significance
rs371198933	20:25,462,631	G/A	—	uncertain significance
rs6138584	20:25,463,148	T/A	intron variant	—
rs1298023886	20:25,469,915	C/T	—	uncertain significance
rs144999465	20:25,469,920	C/T	—	likely benign
rs2516621245	20:25,469,927	C/G	—	uncertain significance
rs550349247	20:25,470,560	C/A	—	uncertain significance
rs532206567	20:25,472,013	G/A	—	uncertain significance
rs2516655201	20:25,472,027	T/C	—	uncertain significance
rs368408445	20:25,472,039	C/T	—	uncertain significance
rs971462541	20:25,472,052	A/C	—	uncertain significance
rs567610080	20:25,472,061	C/T	—	uncertain significance
rs778013280	20:25,472,066	C/G	—	uncertain significance
rs771285325	20:25,472,090	A/T	—	uncertain significance
rs141376094	20:25,472,105	G/A	—	benign
rs2516711066	20:25,477,346	C/T	—	uncertain significance
rs200128495	20:25,477,390	G/C	—	uncertain significance
rs150847797	20:25,477,410	C/T	—	uncertain significance
rs377727308	20:25,477,411	G/A	—	uncertain significance
rs1296126400	20:25,478,883	C/T	—	uncertain significance
rs746614158	20:25,478,895	C/T	—	likely benign
rs140736402	20:25,481,559	C/T	—	uncertain significance
rs1185062802	20:25,481,627	C/T	—	uncertain significance
rs148396885	20:25,481,639	T/G	—	uncertain significance
rs760489764	20:25,484,646	G/A	—	uncertain significance
rs2516796550	20:25,485,529	T/C	—	uncertain significance
rs557323093	20:25,485,576	T/C	—	uncertain significance
rs117522200	20:25,485,580	C/G	—	uncertain significance
rs143641080	20:25,485,604	C/T	—	conflicting classifications of pathogenicity
rs1254409601	20:25,485,624	C/T	—	uncertain significance
rs762025575	20:25,485,628	G/A	—	uncertain significance
rs138824564	20:25,485,663	C/T	—	uncertain significance
rs570501450	20:25,491,372	G/C	—	uncertain significance
rs139869636	20:25,493,496	G/A	—	uncertain significance
rs201891720	20:25,493,559	C/T	—	likely benign
rs2516857676	20:25,493,592	C/T	—	uncertain significance
rs572913298	20:25,493,609	T/C	—	likely benign
rs904950980	20:25,493,616	A/T	—	uncertain significance
rs1161615674	20:25,498,428	C/T	—	uncertain significance
rs403152	20:25,505,567	G/A	intron variant	—

Showing 100 of 106 variants. Use the SNP search for the full list.

Gene information from NCBI Gene. Variant classifications from ClinVar.