ATG2B

autophagy related 2B

Summary

This gene encodes a protein required for autophagy. The encoded protein is involved in autophagosome formation. A germline duplication of a region that includes this gene is associated with predisposition to myeloid malignancies. [provided by RefSeq, Jul 2016]

Known Variants222 total

rsid	Position (GRCh37)	Alleles	Class	ClinVar
rs775986319	14:96,752,124	C/T	—	uncertain significance
rs151219519	14:96,752,161	G/A	—	likely benign
rs139161893	14:96,752,172	C/T	—	uncertain significance
rs377132770	14:96,752,179	C/T	—	likely benign
rs1019231132	14:96,752,223	G/C	—	uncertain significance
rs201349483	14:96,752,231	C/T	—	uncertain significance
rs145257288	14:96,752,300	G/C	—	uncertain significance
rs10141328	14:96,752,555	T/C	—	benign
rs17093991	14:96,752,584	G/A	—	benign
rs12148011	14:96,755,719	G/A	—	benign
rs75597833	14:96,755,809	A/G	—	benign
rs185816070	14:96,756,015	T/C	—	uncertain significance
rs144991946	14:96,756,058	G/C	—	likely benign
rs146775079	14:96,756,067	G/A	—	uncertain significance
rs765725852	14:96,756,070	A/C	—	uncertain significance
rs35258365	14:96,756,094	T/C	—	benign
rs114552965	14:96,756,325	A/T	—	benign
rs201940277	14:96,756,794	G/T	—	uncertain significance
rs200959600	14:96,756,824	C/T	—	likely benign
rs751967764	14:96,756,870	C/T	—	uncertain significance
rs77294752	14:96,756,973	T/C	—	benign
rs1422192627	14:96,757,169	G/A	—	uncertain significance
rs778385045	14:96,757,262	C/T	—	uncertain significance
rs10454690	14:96,757,361	T/A	—	benign
rs1886486250	14:96,757,958	T/C	—	uncertain significance
rs143473070	14:96,757,985	T/C	—	uncertain significance
rs2275022	14:96,758,160	C/T	—	benign
rs953224520	14:96,758,421	G/A	—	uncertain significance
rs6575580	14:96,758,665	G/A	—	benign
rs1889378	14:96,761,086	C/G	—	benign
rs144643846	14:96,761,336	G/A	—	uncertain significance
rs1247813551	14:96,761,441	T/A	—	uncertain significance
rs150055658	14:96,761,445	T/C	—	likely benign
rs772195120	14:96,761,459	T/C	—	uncertain significance
rs45468796	14:96,761,514	T/A	—	benign
rs1770547	14:96,761,557	A/C	—	benign
rs1886612173	14:96,761,825	G/A	—	uncertain significance
rs140123887	14:96,761,937	A/G	—	benign
rs141704194	14:96,768,316	C/T	—	benign
rs150538996	14:96,768,335	G/A	—	benign
rs368514043	14:96,768,374	C/T	—	likely benign
rs74719094	14:96,768,380	T/G	—	benign
rs146815375	14:96,768,424	C/T	—	uncertain significance
rs117481952	14:96,768,425	G/A	—	benign
rs1362699853	14:96,768,432	G/C	—	uncertain significance
rs112609665	14:96,768,673	C/T	—	benign
rs1280498	14:96,768,751	A/T	—	benign
rs972726	14:96,769,233	A/G	—	benign
rs2275020	14:96,769,380	G/A	—	benign
rs370449015	14:96,769,402	T/C	—	uncertain significance
rs1454755271	14:96,769,512	C/A	—	uncertain significance
rs35682045	14:96,769,536	G/A	—	benign
rs114955360	14:96,769,566	C/T	—	benign
rs370728333	14:96,769,567	G/A	—	uncertain significance
rs149087645	14:96,769,601	G/A	—	benign
rs8007718	14:96,770,720	T/G	—	benign
rs760594642	14:96,770,863	T/C	—	uncertain significance
rs141740422	14:96,770,893	T/C	—	uncertain significance
rs201971971	14:96,770,897	G/A	—	uncertain significance
rs145906587	14:96,770,908	G/T	—	uncertain significance
rs780365806	14:96,770,912	G/T	—	uncertain significance
rs377092086	14:96,770,926	G/A	—	uncertain significance
rs369023445	14:96,770,928	A/C	—	uncertain significance
rs3742474	14:96,771,130	C/T	—	benign
rs202049106	14:96,771,953	G/A	—	uncertain significance
rs923075284	14:96,772,019	C/T	—	uncertain significance
rs1283115479	14:96,772,029	G/A	—	uncertain significance
rs748996774	14:96,772,054	G/C	—	uncertain significance
rs199803616	14:96,772,057	C/T	—	likely benign
rs72704878	14:96,772,059	T/A	—	likely benign
rs765569547	14:96,772,063	G/A	—	likely benign
rs763093217	14:96,772,074	C/T	—	uncertain significance
rs146028674	14:96,772,075	G/A	—	likely benign
rs201130552	14:96,772,091	T/C	—	likely benign
rs2289623	14:96,772,330	A/C	—	benign
rs55845548	14:96,772,907	C/A	—	benign
rs72704880	14:96,772,942	C/T	—	benign
rs1020780622	14:96,773,058	G/A	—	uncertain significance
rs1220864469	14:96,773,114	C/A	—	uncertain significance
rs1886962646	14:96,773,157	G/C	—	uncertain significance
rs143695335	14:96,773,164	A/G	—	benign
rs146800472	14:96,773,189	G/A	—	benign
rs1156339225	14:96,773,229	A/C	—	uncertain significance
rs34869733	14:96,773,389	C/T	—	benign
rs2289626	14:96,775,613	T/G	—	benign
rs2504115851	14:96,775,853	T/G	—	uncertain significance
rs202041291	14:96,775,864	C/T	—	uncertain significance
rs2504115980	14:96,775,930	A/G	—	uncertain significance
rs2289628	14:96,776,008	A/G	—	benign
rs3759602	14:96,777,408	T/C	—	benign
rs778335132	14:96,777,450	G/A	—	likely benign
rs3759601	14:96,777,468	G/C	missense variant	benign
rs147079514	14:96,777,536	A/G	—	benign
rs966598987	14:96,777,557	C/T	—	uncertain significance
rs201939755	14:96,777,572	G/A	—	uncertain significance
rs756276197	14:96,777,579	T/C	—	likely benign
rs776280548	14:96,777,620	T/C	—	uncertain significance
rs1887157802	14:96,777,921	C/A	—	uncertain significance
rs769584848	14:96,777,939	C/G	—	uncertain significance
rs773984669	14:96,777,946	C/T	—	uncertain significance

Showing 100 of 222 variants. Use the SNP search for the full list.

Gene information from NCBI Gene. Variant classifications from ClinVar.