LMF1

lipase maturation factor 1

Summary

Involved in triglyceride metabolic process. Predicted to be located in endoplasmic reticulum and membrane. Predicted to be active in endoplasmic reticulum membrane. Implicated in familial lipase maturation factor 1 deficiency. [provided by Alliance of Genome Resources, Jul 2025]

Known Variants529 total

rsid	Position (GRCh37)	Alleles	Class	ClinVar
rs114890365	16:904,236	C/T	—	likely benign
rs75476513	16:904,301	G/T	—	likely benign
rs78699640	16:904,358	G/T	—	likely benign
rs147193806	16:904,395	C/T	—	likely benign
rs1226297892	16:904,538	G/A	—	likely benign
rs2544422379	16:904,540	G/A	—	uncertain significance
rs750381542	16:904,542	C/A	—	uncertain significance
rs779769803	16:904,544	G/A	—	likely benign
rs1289224838	16:904,547	C/T	—	likely benign
rs199591347	16:904,548	A/C	—	likely benign
rs4984948	16:904,551	G/C	—	benign
rs1414737004	16:904,559	A/G	—	likely benign
rs199544373	16:904,561	G/A	—	uncertain significance
rs2069136008	16:904,563	T/C	—	uncertain significance
rs913911840	16:904,574	G/C	—	likely benign
rs751822327	16:904,585	C/T	—	uncertain significance
rs767415527	16:904,591	G/C	—	uncertain significance
rs750316655	16:904,598	C/T	—	likely benign
rs199843015	16:904,599	G/C	—	uncertain significance
rs747840267	16:904,616	G/A	—	conflicting classifications of pathogenicity
rs746347412	16:904,625	C/T	—	likely benign
rs533542876	16:904,626	C/T	—	uncertain significance
rs555435528	16:904,627	G/T	—	likely benign
rs201012186	16:904,628	C/A	—	likely benign
rs1395199265	16:904,630	C/T	—	uncertain significance
rs190958016	16:904,643	C/G	—	benign
rs751666631	16:904,645	C/T	—	uncertain significance
rs774434840	16:904,648	C/T	—	uncertain significance
rs762154063	16:904,649	G/A	—	likely benign
rs560030260	16:904,652	G/A	—	likely benign
rs980936802	16:904,661	C/T	—	likely benign
rs200159114	16:904,662	C/T	—	uncertain significance
rs151137164	16:904,668	C/T	—	benign
rs758116895	16:904,669	G/A	—	uncertain significance
rs1414836944	16:904,670	G/A	—	likely benign
rs2151673189	16:904,671	C/A	—	uncertain significance
rs368273483	16:904,676	C/T	—	likely benign
rs1432924219	16:904,682	C/T	—	likely benign
rs2544423581	16:904,683	C/T	—	uncertain significance
rs756488965	16:904,684	T/C	—	uncertain significance
rs780474952	16:904,688	G/A	—	likely benign
rs749862939	16:904,691	C/T	—	likely benign
rs372151515	16:904,694	T/C	—	likely benign
rs748287562	16:904,698	C/T	—	uncertain significance
rs200676184	16:904,706	C/T	—	uncertain significance
rs373526378	16:904,715	G/A	—	likely benign
rs367769866	16:904,721	A/G	—	likely benign
rs9925991	16:904,871	G/A	—	benign
rs116811949	16:904,929	G/A	—	likely benign
rs1188030413	16:905,774	T/C	—	likely benign
rs1000355362	16:906,079	G/C	—	uncertain significance
rs148566486	16:914,220	T/G	intron variant	—
rs746596358	16:918,784	G/C	—	benign
rs188092927	16:918,841	C/T	—	likely benign
rs111431282	16:918,870	T/C	—	likely benign
rs149923445	16:918,924	C/T	—	benign
rs765586986	16:918,938	T/C	—	uncertain significance
rs2544486376	16:918,945	T/C	—	uncertain significance
rs989431710	16:918,948	G/T	—	uncertain significance
rs777964574	16:918,949	C/T	—	likely benign
rs781503559	16:918,952	G/A	—	likely benign
rs746145984	16:918,955	C/A	—	uncertain significance
rs375221245	16:918,961	C/T	—	likely benign
rs369478194	16:918,962	G/A	—	conflicting classifications of pathogenicity
rs749219178	16:918,963	C/T	—	uncertain significance
rs1206413071	16:918,964	G/A	—	likely benign
rs768541855	16:918,971	T/A	—	uncertain significance
rs747600410	16:918,977	G/A	—	uncertain significance
rs376340194	16:918,992	G/C	—	uncertain significance
rs2544486692	16:918,994	C/G	—	uncertain significance
rs145008721	16:918,996	C/T	—	likely benign
rs142258761	16:918,997	G/A	—	likely benign
rs775754688	16:918,999	C/T	—	uncertain significance
rs62012416	16:919,000	G/A	—	likely benign
rs532127028	16:919,002	C/T	—	conflicting classifications of pathogenicity
rs34934602	16:919,003	G/A	—	likely benign
rs757412243	16:919,011	G/A	—	likely benign
rs2069695087	16:919,013	A/G	—	uncertain significance
rs1181212853	16:919,022	G/A	—	uncertain significance
rs372490098	16:919,030	G/C	—	uncertain significance
rs778756884	16:919,032	T/C	—	uncertain significance
rs377384616	16:919,041	C/T	—	uncertain significance
rs772646362	16:919,042	G/A	—	likely benign
rs746641073	16:919,046	T/G	—	uncertain significance
rs549735506	16:919,050	C/T	—	uncertain significance
rs763350006	16:919,051	G/A	—	likely benign
rs750431140	16:919,072	G/A	—	likely benign
rs1006906151	16:919,503	G/A	—	benign
rs115550520	16:919,659	G/T	—	likely benign
rs61282928	16:919,667	C/T	—	benign
rs147995699	16:919,668	G/A	—	likely benign
rs138911395	16:919,859	C/T	—	likely benign
rs367631358	16:919,863	C/T	—	likely benign
rs114354808	16:919,870	G/A	—	likely benign
rs142224154	16:919,874	G/A	—	benign
rs755055115	16:919,876	C/A	—	uncertain significance
rs775682133	16:919,892	C/T	—	likely benign
rs574656841	16:919,893	G/A	—	uncertain significance
rs181731943	16:919,894	C/T	—	conflicting classifications of pathogenicity
rs371869557	16:919,895	G/A	—	likely benign

Showing 100 of 529 variants. Use the SNP search for the full list.

Gene information from NCBI Gene. Variant classifications from ClinVar.