MDN1

midasin AAA ATPase 1

Summary

Predicted to enable ATP binding activity and ATP hydrolysis activity. Involved in ribosomal large subunit assembly. Located in cytosol; intermediate filament cytoskeleton; and nuclear lumen. [provided by Alliance of Genome Resources, Jul 2025]

Known Variants401 total

rsid	Position (GRCh37)	Alleles	Class	ClinVar
rs770944096	6:90,353,794	G/A	—	uncertain significance
rs774441685	6:90,353,795	C/T	—	uncertain significance
rs2536109836	6:90,353,870	C/T	—	uncertain significance
rs1808330356	6:90,353,912	C/G	—	uncertain significance
rs140050356	6:90,354,735	C/A	—	uncertain significance
rs34750131	6:90,354,789	G/A	—	benign
rs112928258	6:90,356,252	A/G	—	benign
rs375185709	6:90,356,292	C/G	—	uncertain significance
rs34703897	6:90,357,811	G/A	—	benign
rs2536118646	6:90,357,812	T/C	—	uncertain significance
rs757848323	6:90,359,750	G/A	—	uncertain significance
rs769909838	6:90,359,894	C/T	—	uncertain significance
rs368019786	6:90,360,444	G/A	—	likely benign
rs531060521	6:90,360,482	T/C	—	uncertain significance
rs140535277	6:90,360,559	A/G	—	likely benign
rs150459823	6:90,361,933	C/T	—	likely benign
rs138455168	6:90,362,755	T/C	—	uncertain significance
rs1047136610	6:90,362,822	T/C	—	likely benign
rs149359389	6:90,362,832	T/G	—	uncertain significance
rs777064501	6:90,362,835	G/T	—	uncertain significance
rs1229599224	6:90,363,873	C/T	—	likely benign
rs749597028	6:90,363,887	G/A	—	likely benign
rs2536133885	6:90,363,933	A/G	—	uncertain significance
rs1363098877	6:90,364,021	T/C	—	uncertain significance
rs2536137424	6:90,365,510	T/G	—	uncertain significance
rs919752472	6:90,365,531	A/C	—	uncertain significance
rs763726088	6:90,365,533	G/A	—	uncertain significance
rs377465597	6:90,365,577	C/G	—	uncertain significance
rs145293582	6:90,365,595	C/T	—	likely benign
rs775106114	6:90,365,614	C/T	—	uncertain significance
rs1287401379	6:90,366,423	G/C	—	uncertain significance
rs115791795	6:90,366,471	G/A	—	likely benign
rs899227946	6:90,366,508	C/T	—	uncertain significance
rs114504442	6:90,367,954	C/T	—	uncertain significance
rs145493272	6:90,367,955	G/A	—	likely benign
rs148852520	6:90,367,972	T/C	—	likely benign
rs771559557	6:90,368,002	C/T	—	uncertain significance
rs143737232	6:90,368,013	C/G	—	uncertain significance
rs375910560	6:90,368,062	T/C	—	uncertain significance
rs748641567	6:90,368,377	A/C	—	uncertain significance
rs770320485	6:90,368,379	C/T	—	uncertain significance
rs34732313	6:90,368,380	G/A	—	benign
rs139030773	6:90,368,431	T/A	—	uncertain significance
rs115080892	6:90,368,593	A/C	—	benign
rs149587926	6:90,368,594	C/T	—	uncertain significance
rs757658620	6:90,368,603	T/A	—	uncertain significance
rs758790454	6:90,368,628	G/T	—	uncertain significance
rs202049803	6:90,371,158	T/C	—	benign
rs114646660	6:90,371,215	C/T	—	benign
rs925865944	6:90,371,222	G/A	—	uncertain significance
rs2128301352	6:90,371,813	A/G	—	uncertain significance
rs2536153133	6:90,371,815	T/C	—	likely benign
rs560611249	6:90,371,829	T/C	—	uncertain significance
rs1253505612	6:90,371,851	A/C	—	uncertain significance
rs374582290	6:90,371,877	C/T	—	uncertain significance
rs765432930	6:90,372,561	C/T	—	uncertain significance
rs759393935	6:90,372,571	C/A	—	likely benign
rs36040566	6:90,372,574	A/C	—	benign
rs760564111	6:90,372,577	A/C	—	uncertain significance
rs780660286	6:90,372,623	T/C	—	uncertain significance
rs146464056	6:90,372,654	C/T	—	uncertain significance
rs957745680	6:90,374,241	T/G	—	uncertain significance
rs115635255	6:90,374,281	T/C	—	uncertain significance
rs16882046	6:90,374,283	A/G	—	benign
rs1810385880	6:90,377,746	C/A	—	uncertain significance
rs148084650	6:90,377,802	A/G	—	likely benign
rs35906591	6:90,377,845	A/G	—	benign
rs759752648	6:90,380,697	G/A	—	uncertain significance
rs768870809	6:90,381,935	G/A	—	uncertain significance
rs138617275	6:90,382,002	C/T	—	likely benign
rs905125848	6:90,382,010	G/A	—	uncertain significance
rs115238428	6:90,382,021	G/A	—	likely benign
rs776982962	6:90,382,030	G/C	—	uncertain significance
rs79087127	6:90,382,295	G/C	—	benign
rs376749129	6:90,382,298	T/G	—	uncertain significance
rs769923782	6:90,382,350	G/T	—	uncertain significance
rs6929989	6:90,382,405	G/A	—	benign
rs528313135	6:90,382,414	T/G	—	uncertain significance
rs2536179225	6:90,382,979	G/T	—	uncertain significance
rs781175774	6:90,383,009	T/C	—	likely benign
rs199615065	6:90,383,024	C/T	—	uncertain significance
rs201906884	6:90,383,034	A/G	—	likely benign
rs2536179417	6:90,383,068	T/C	—	uncertain significance
rs749157730	6:90,383,845	A/G	—	uncertain significance
rs114130059	6:90,383,869	C/T	—	likely benign
rs753798288	6:90,383,950	G/A	—	uncertain significance
rs369011833	6:90,383,956	G/A	—	uncertain significance
rs777152046	6:90,383,997	T/G	—	uncertain significance
rs369156050	6:90,384,006	T/C	—	uncertain significance
rs767668592	6:90,384,038	A/G	—	likely benign
rs750311342	6:90,384,052	T/C	—	uncertain significance
rs114236310	6:90,384,082	G/A	—	benign
rs748656784	6:90,384,088	G/T	—	uncertain significance
rs774668187	6:90,384,121	C/G	—	uncertain significance
rs1020390960	6:90,384,132	C/A	—	uncertain significance
rs766037169	6:90,384,205	G/A	—	uncertain significance
rs35134619	6:90,384,228	T/C	—	uncertain significance
rs1181789138	6:90,384,234	G/C	—	uncertain significance
rs200401363	6:90,384,257	C/A	—	uncertain significance
rs41273327	6:90,384,274	T/C	—	benign

Showing 100 of 401 variants. Use the SNP search for the full list.

Gene information from NCBI Gene. Variant classifications from ClinVar.