ARMC9

armadillo repeat containing 9

Summary

Predicted to be involved in cilium assembly and positive regulation of smoothened signaling pathway. Located in centriole and ciliary basal body. Implicated in Joubert syndrome 30. [provided by Alliance of Genome Resources, Jul 2025]

Known Variants567 total

rsid	Position (GRCh37)	Alleles	Class	ClinVar
rs74651652	2:232,070,906	T/C	—	benign
rs61753914	2:232,070,961	A/G	—	benign
rs376958829	2:232,070,964	C/G	—	uncertain significance
rs2469577572	2:232,070,967	G/C	—	uncertain significance
rs200925709	2:232,070,970	C/T	—	uncertain significance
rs774906944	2:232,070,976	T/C	—	uncertain significance
rs767650589	2:232,070,986	T/C	—	uncertain significance
rs1114167447	2:232,071,007	G/T	—	conflicting classifications of pathogenicity
rs1459107569	2:232,071,010	T/A	—	likely benign
rs760205337	2:232,071,017	C/G	—	likely benign
rs373735875	2:232,071,022	C/T	—	likely benign
rs370983173	2:232,072,822	A/C	—	benign
rs2125309272	2:232,072,829	A/T	—	likely benign
rs1445045272	2:232,072,863	A/G	—	likely benign
rs778975833	2:232,072,864	G/C	—	uncertain significance
rs1330612935	2:232,072,888	G/T	—	pathogenic
rs200364288	2:232,072,898	T/C	—	uncertain significance
rs11558174	2:232,072,912	T/C	—	benign
rs1366767809	2:232,072,925	T/G	—	uncertain significance
rs35643982	2:232,072,929	C/T	—	benign
rs759105498	2:232,072,930	G/A	—	uncertain significance
rs2469584088	2:232,072,942	G/A	—	uncertain significance
rs2469584099	2:232,072,947	C/G	—	likely benign
rs2032317356	2:232,072,954	T/C	—	likely benign
rs2125309600	2:232,072,955	T/C	—	uncertain significance
rs1214948838	2:232,072,964	A/G	—	uncertain significance
rs12465438	2:232,073,106	G/A	—	benign
rs185997237	2:232,079,527	T/C	—	likely benign
rs2469601478	2:232,079,533	C/T	—	likely benign
rs747328656	2:232,079,539	C/T	—	likely benign
rs1356971637	2:232,079,541	C/T	—	uncertain significance
rs1248147660	2:232,079,542	A/G	—	likely pathogenic
rs781417301	2:232,079,543	G/A	—	likely pathogenic
rs1260591633	2:232,079,545	A/T	—	uncertain significance
rs200269213	2:232,079,555	C/T	—	likely benign
rs144388331	2:232,079,556	G/A	—	uncertain significance
rs368431189	2:232,079,557	C/T	—	uncertain significance
rs2125321079	2:232,079,566	A/G	—	uncertain significance
rs143756333	2:232,079,570	C/T	—	likely benign
rs750247691	2:232,079,571	G/A	missense variant	pathogenic
rs974916571	2:232,079,588	C/T	—	likely benign
rs780518289	2:232,079,591	C/T	—	likely benign
rs759705369	2:232,079,592	G/C	—	uncertain significance
rs758536951	2:232,079,610	A/T	—	uncertain significance
rs752044276	2:232,079,615	A/C	—	likely benign
rs140272259	2:232,079,620	C/T	—	uncertain significance
rs746287033	2:232,079,622	A/C	—	uncertain significance
rs372770167	2:232,079,625	C/A	synonymous variant	likely benign
rs563490038	2:232,079,626	G/A	—	uncertain significance
rs2033331258	2:232,079,644	C/T	—	uncertain significance
rs376271713	2:232,079,647	A/G	—	uncertain significance
rs2125321327	2:232,079,654	G/A	—	likely benign
rs2125321335	2:232,079,657	A/G	—	likely benign
rs772969644	2:232,079,662	A/G	—	uncertain significance
rs2125321345	2:232,079,664	C/G	—	uncertain significance
rs199768804	2:232,079,682	A/G	—	uncertain significance
rs2125321410	2:232,079,696	G/A	—	likely benign
rs2033337581	2:232,079,701	C/T	—	uncertain significance
rs757763630	2:232,079,715	G/A	—	likely pathogenic
rs113547151	2:232,079,724	C/G	—	likely benign
rs780579882	2:232,079,727	G/A	—	likely benign
rs2469602527	2:232,079,728	G/A	—	likely benign
rs754616310	2:232,079,734	C/T	—	likely benign
rs760110590	2:232,081,347	C/G	—	likely benign
rs371282155	2:232,081,362	G/C	—	uncertain significance
rs766807315	2:232,081,365	G/A	—	likely benign
rs201901213	2:232,081,369	G/A	—	conflicting classifications of pathogenicity
rs1172299192	2:232,081,375	A/T	—	uncertain significance
rs747685163	2:232,081,397	T/G	—	uncertain significance
rs746880469	2:232,081,408	G/A	—	uncertain significance
rs2469606714	2:232,081,411	G/A	—	uncertain significance
rs2125324051	2:232,081,412	C/T	—	uncertain significance
rs2125324057	2:232,081,415	C/T	—	uncertain significance
rs2469606739	2:232,081,416	C/G	—	likely benign
rs2033542555	2:232,081,430	C/G	—	uncertain significance
rs2469606831	2:232,081,441	C/T	—	uncertain significance
rs2469606852	2:232,081,446	C/G	—	uncertain significance
rs532584474	2:232,081,451	C/G	—	uncertain significance
rs1027349978	2:232,081,458	T/G	—	likely benign
rs2125324133	2:232,081,462	G/A	—	uncertain significance
rs886764569	2:232,081,472	C/T	—	uncertain significance
rs2469607032	2:232,081,480	C/T	—	uncertain significance
rs772213189	2:232,081,482	C/T	—	likely benign
rs2469607069	2:232,081,485	C/T	—	likely benign
rs1405827524	2:232,081,489	T/A	—	uncertain significance
rs1157757818	2:232,081,490	T/A	—	uncertain significance
rs2469607142	2:232,081,495	G/A	—	uncertain significance
rs1455055967	2:232,081,496	A/G	—	uncertain significance
rs761213261	2:232,081,497	A/G	—	likely benign
rs1381984174	2:232,081,519	T/A	—	likely benign
rs140335093	2:232,081,523	A/G	—	likely benign
rs10202295	2:232,084,411	T/G	intron variant	—
rs557378073	2:232,087,421	T/G	—	likely benign
rs745666268	2:232,087,424	T/C	—	likely benign
rs1230311470	2:232,087,429	T/G	—	likely benign
rs138398575	2:232,087,444	T/G	—	likely benign
rs1468038129	2:232,087,456	G/C	—	uncertain significance
rs2125334112	2:232,087,466	T/C	—	uncertain significance
rs951972543	2:232,087,473	G/C	—	uncertain significance
rs1626450	2:232,087,474	A/G	—	benign

Showing 100 of 567 variants. Use the SNP search for the full list.

Gene information from NCBI Gene. Variant classifications from ClinVar.