ATG2A

autophagy related 2A

Summary

Enables lipid transfer activity. Involved in autophagosome assembly and positive regulation of autophagosome assembly. Is active in organelle membrane contact site. [provided by Alliance of Genome Resources, Jul 2025]

Known Variants144 total

rsid	Position (GRCh37)	Alleles	Class	ClinVar
rs2497912891	11:64,662,505	A/C	—	uncertain significance
rs770497554	11:64,662,515	C/T	—	uncertain significance
rs2497913067	11:64,662,533	C/T	—	likely benign
rs751327728	11:64,662,548	G/A	—	uncertain significance
rs139262108	11:64,662,575	G/A	—	uncertain significance
rs1477315197	11:64,662,590	C/T	—	uncertain significance
rs750008738	11:64,662,614	G/C	—	uncertain significance
rs200184532	11:64,662,835	C/T	—	uncertain significance
rs762126437	11:64,662,836	G/A	—	uncertain significance
rs140343176	11:64,662,850	T/A	—	uncertain significance
rs535616947	11:64,662,863	G/A	—	uncertain significance
rs148192310	11:64,662,869	C/T	—	benign
rs761347922	11:64,663,954	G/A	—	uncertain significance
rs778296755	11:64,664,013	T/C	—	uncertain significance
rs1398576131	11:64,664,026	T/G	—	uncertain significance
rs202081004	11:64,664,239	C/T	—	uncertain significance
rs147085310	11:64,664,918	C/G	—	uncertain significance
rs775727990	11:64,665,160	C/T	—	uncertain significance
rs1315252823	11:64,665,199	A/G	—	uncertain significance
rs374503749	11:64,665,201	G/A	—	uncertain significance
rs201777332	11:64,665,390	C/T	—	uncertain significance
rs751418069	11:64,665,443	C/T	—	likely benign
rs144918427	11:64,665,585	C/T	—	likely benign
rs772069729	11:64,665,597	C/T	—	uncertain significance
rs1407057390	11:64,665,768	C/T	—	uncertain significance
rs776977388	11:64,665,770	C/T	—	uncertain significance
rs748397030	11:64,666,193	C/T	—	uncertain significance
rs142230025	11:64,666,212	C/T	—	uncertain significance
rs375430002	11:64,666,265	G/T	—	uncertain significance
rs145407425	11:64,666,318	T/C	—	likely benign
rs762113071	11:64,668,018	T/C	—	uncertain significance
rs147598848	11:64,668,060	C/T	—	uncertain significance
rs765732642	11:64,668,061	G/A	—	uncertain significance
rs748412226	11:64,668,076	T/C	—	uncertain significance
rs142058668	11:64,668,405	C/T	—	uncertain significance
rs539616678	11:64,668,516	C/T	—	likely benign
rs368325120	11:64,669,449	G/A	—	likely benign
rs1354642101	11:64,669,453	G/A	—	uncertain significance
rs374942063	11:64,669,546	C/T	—	uncertain significance
rs776789973	11:64,669,580	G/C	—	uncertain significance
rs747927573	11:64,669,595	G/A	—	uncertain significance
rs765611102	11:64,669,735	A/G	—	uncertain significance
rs200968741	11:64,669,761	C/T	—	uncertain significance
rs142840100	11:64,669,794	C/T	—	uncertain significance
rs146082220	11:64,669,812	G/A	—	likely benign
rs752478622	11:64,669,822	G/C	—	uncertain significance
rs1944382001	11:64,669,847	A/T	—	uncertain significance
rs766832311	11:64,670,022	C/G	—	uncertain significance
rs754243437	11:64,670,028	G/C	—	uncertain significance
rs1171984610	11:64,670,029	G/T	—	uncertain significance
rs145632022	11:64,670,056	C/T	—	uncertain significance
rs200061014	11:64,670,137	C/G	—	uncertain significance
rs759628876	11:64,670,771	C/T	—	uncertain significance
rs1944425111	11:64,670,809	A/C	—	uncertain significance
rs373100138	11:64,671,064	C/T	—	uncertain significance
rs1219593330	11:64,671,082	T/A	—	uncertain significance
rs372022314	11:64,673,107	C/T	—	uncertain significance
rs773884095	11:64,673,108	G/A	—	uncertain significance
rs141049352	11:64,673,278	A/G	—	uncertain significance
rs201916479	11:64,673,302	C/T	—	uncertain significance
rs983657597	11:64,673,605	C/T	—	uncertain significance
rs368274949	11:64,673,619	T/G	—	uncertain significance
rs200110832	11:64,673,646	C/T	—	uncertain significance
rs2498016020	11:64,673,858	T/G	—	uncertain significance
rs752541532	11:64,673,897	C/T	—	uncertain significance
rs968290673	11:64,673,931	T/C	—	uncertain significance
rs776248968	11:64,673,948	G/A	—	uncertain significance
rs142738692	11:64,673,964	G/A	—	uncertain significance
rs370816722	11:64,673,997	C/G	—	uncertain significance
rs370733242	11:64,674,000	C/T	—	conflicting classifications of pathogenicity
rs2498020443	11:64,674,167	C/T	—	uncertain significance
rs768440291	11:64,674,824	G/A	—	uncertain significance
rs141282404	11:64,674,834	C/T	—	uncertain significance
rs375290726	11:64,674,863	G/A	—	uncertain significance
rs61741398	11:64,675,074	G/A	—	benign
rs202213951	11:64,675,078	C/T	—	uncertain significance
rs140012093	11:64,675,127	G/A	—	benign
rs1274363634	11:64,675,254	G/C	—	uncertain significance
rs778632862	11:64,676,519	G/A	—	uncertain significance
rs1354005701	11:64,676,590	C/A	—	uncertain significance
rs182626621	11:64,676,780	C/A	—	uncertain significance
rs145534182	11:64,676,797	C/T	—	uncertain significance
rs1474157059	11:64,676,836	A/G	—	likely benign
rs777053187	11:64,676,839	C/A	—	uncertain significance
rs774408869	11:64,677,162	C/T	—	uncertain significance
rs751061098	11:64,677,201	C/T	—	uncertain significance
rs151296650	11:64,677,218	T/C	—	uncertain significance
rs61746812	11:64,677,270	C/T	—	benign
rs61746813	11:64,677,273	C/G	—	uncertain significance
rs2498056308	11:64,677,289	G/C	—	uncertain significance
rs1944696380	11:64,677,306	G/T	—	uncertain significance
rs200244363	11:64,677,310	G/A	—	likely benign
rs758825597	11:64,677,335	G/A	—	uncertain significance
rs564922823	11:64,677,341	C/A	—	uncertain significance
rs367636075	11:64,677,365	G/A	—	uncertain significance
rs781153736	11:64,677,552	C/T	—	likely benign
rs750968916	11:64,677,580	C/A	—	uncertain significance
rs745833839	11:64,677,657	C/T	—	uncertain significance
rs373750405	11:64,677,661	G/A	—	uncertain significance
rs768402770	11:64,677,663	C/T	—	uncertain significance

Showing 100 of 144 variants. Use the SNP search for the full list.

Gene information from NCBI Gene. Variant classifications from ClinVar.