EML6

EMAP like 6

Summary

Predicted to enable microtubule binding activity. Predicted to be located in cytoplasm and microtubule. [provided by Alliance of Genome Resources, Jul 2025]

Known Variants160 total

rsid	Position (GRCh37)	Alleles	Class	ClinVar
rs2549606181	2:54,952,215	C/T	—	uncertain significance
rs544855116	2:54,952,374	G/A	—	uncertain significance
rs76382474	2:54,954,769	C/G	intron variant	—
rs78667279	2:54,957,709	G/A	intron variant	—
rs568317811	2:54,965,334	C/T	—	—
rs535531538	2:54,965,644	C/T	—	—
rs67617923	2:54,968,517	G/A	intron variant	—
rs72806698	2:54,969,379	C/T	downstream gene variant	—
rs17046310	2:54,993,998	C/T	intron variant	—
rs72917514	2:55,013,646	G/A	regulatory region variant	—
rs2549694946	2:55,040,383	C/G	—	uncertain significance
rs1259983687	2:55,040,392	C/G	—	uncertain significance
rs145889900	2:55,040,490	C/T	—	uncertain significance
rs756771011	2:55,043,984	G/A	—	uncertain significance
rs79419424	2:55,049,749	C/T	intron variant	—
rs1341510552	2:55,054,704	T/G	—	uncertain significance
rs1276717319	2:55,054,710	C/G	—	uncertain significance
rs777100783	2:55,054,758	C/T	—	uncertain significance
rs760093873	2:55,054,772	A/T	—	uncertain significance
rs116185852	2:55,054,837	C/T	—	benign
rs2549716997	2:55,056,486	T/A	—	uncertain significance
rs1668751260	2:55,056,504	G/A	—	uncertain significance
rs1425292691	2:55,056,546	G/A	—	uncertain significance
rs367997357	2:55,056,572	A/G	—	uncertain significance
rs778702813	2:55,056,583	T/G	—	uncertain significance
rs189974416	2:55,064,143	G/A	intron variant	—
rs774844351	2:55,071,219	C/T	—	uncertain significance
rs962097491	2:55,071,220	G/A	—	uncertain significance
rs762271942	2:55,071,237	C/G	—	uncertain significance
rs947774999	2:55,071,249	A/G	—	uncertain significance
rs374203536	2:55,071,268	G/A	—	uncertain significance
rs1052231919	2:55,071,312	G/T	—	uncertain significance
rs758364048	2:55,071,339	C/T	—	uncertain significance
rs2549741841	2:55,071,355	C/T	—	uncertain significance
rs76620146	2:55,071,768	A/G	intron variant	—
rs1297670159	2:55,074,641	T/G	—	uncertain significance
rs912317815	2:55,074,691	C/A	—	uncertain significance
rs183064449	2:55,074,709	C/G	—	uncertain significance
rs1345852890	2:55,074,754	G/A	—	uncertain significance
rs1198215051	2:55,077,167	A/T	—	uncertain significance
rs571739337	2:55,077,275	C/T	—	uncertain significance
rs201339209	2:55,077,335	G/A	—	uncertain significance
rs906817693	2:55,080,788	C/A	—	uncertain significance
rs199689214	2:55,080,845	A/G	—	uncertain significance
rs923807837	2:55,080,981	G/T	—	uncertain significance
rs199675739	2:55,080,983	C/G	—	uncertain significance
rs12713280	2:55,081,376	C/A	—	—
rs151096494	2:55,086,689	A/G	—	uncertain significance
rs891922876	2:55,086,745	G/C	—	uncertain significance
rs2549788562	2:55,086,770	A/G	—	uncertain significance
rs767862430	2:55,086,814	G/A	—	uncertain significance
rs766789154	2:55,086,833	C/A	—	uncertain significance
rs2549798338	2:55,090,955	T/G	—	uncertain significance
rs768568521	2:55,090,976	G/A	—	uncertain significance
rs1314337847	2:55,091,022	G/A	—	uncertain significance
rs1478263976	2:55,093,914	A/C	—	uncertain significance
rs189726065	2:55,093,956	C/T	—	benign
rs1424081714	2:55,096,335	G/A	—	uncertain significance
rs1327935099	2:55,096,352	T/C	—	uncertain significance
rs1427957837	2:55,096,407	A/G	—	uncertain significance
rs200497644	2:55,096,447	T/A	—	uncertain significance
rs201615199	2:55,096,488	A/G	—	uncertain significance
rs1306995729	2:55,098,640	G/C	—	uncertain significance
rs1292325161	2:55,098,721	G/C	—	uncertain significance
rs1374651284	2:55,098,735	T/G	—	uncertain significance
rs1037985939	2:55,106,708	T/C	—	uncertain significance
rs561792289	2:55,106,728	A/G	—	uncertain significance
rs996735405	2:55,106,750	A/G	—	uncertain significance
rs191661637	2:55,106,760	A/G	—	likely benign
rs762487049	2:55,106,768	C/T	—	uncertain significance
rs1032213459	2:55,106,770	A/C	—	uncertain significance
rs1008590653	2:55,118,231	C/T	—	uncertain significance
rs372453322	2:55,118,250	T/C	—	uncertain significance
rs1316041037	2:55,118,280	G/T	—	uncertain significance
rs200130756	2:55,118,288	G/A	—	uncertain significance
rs2549858625	2:55,119,606	C/A	—	uncertain significance
rs1324071161	2:55,119,618	C/A	—	uncertain significance
rs972466875	2:55,119,627	G/T	—	uncertain significance
rs1306767958	2:55,119,702	C/T	—	uncertain significance
rs2549859197	2:55,119,714	T/G	—	uncertain significance
rs1469302578	2:55,119,731	C/G	—	uncertain significance
rs889772353	2:55,119,767	G/C	—	uncertain significance
rs200022878	2:55,122,122	C/G	—	uncertain significance
rs369683148	2:55,122,131	T/C	—	uncertain significance
rs2549867741	2:55,122,146	T/G	—	uncertain significance
rs2549867767	2:55,122,154	A/G	—	uncertain significance
rs1672703783	2:55,122,413	T/C	—	uncertain significance
rs561494154	2:55,122,436	A/G	—	uncertain significance
rs1435073437	2:55,122,445	A/G	—	uncertain significance
rs2549869204	2:55,122,523	A/C	—	uncertain significance
rs1328679020	2:55,130,219	T/G	—	uncertain significance
rs763669607	2:55,130,225	G/A	—	uncertain significance
rs375823350	2:55,130,511	C/T	—	uncertain significance
rs895669786	2:55,130,561	A/T	—	uncertain significance
rs201862406	2:55,130,562	A/G	—	uncertain significance
rs369124825	2:55,130,563	C/A	—	uncertain significance
rs1229310348	2:55,130,567	C/T	—	uncertain significance
rs994880615	2:55,130,571	C/T	—	uncertain significance
rs749672759	2:55,130,612	A/C	—	uncertain significance
rs761628241	2:55,138,123	G/A	—	uncertain significance

Showing 100 of 160 variants. Use the SNP search for the full list.

Gene information from NCBI Gene. Variant classifications from ClinVar.