ATRN

attractin

Summary

This gene encodes both membrane-bound and secreted protein isoforms. A membrane-bound isoform exhibits sequence similarity with the mouse mahogany protein, a receptor involved in controlling obesity. A secreted isoform is involved in the initial immune cell clustering during inflammatory responses that may regulate the chemotactic activity of chemokines. [provided by RefSeq, Apr 2016]

Known Variants310 total

rsid	Position (GRCh37)	Alleles	Class	ClinVar
rs758432510	20:3,451,711	T/G	—	likely benign
rs1410443010	20:3,451,768	C/T	—	uncertain significance
rs1347770139	20:3,451,799	G/A	—	likely benign
rs1298391048	20:3,451,807	C/T	—	uncertain significance
rs1401894420	20:3,451,808	G/C	—	likely benign
rs559292386	20:3,451,814	A/C	—	benign
rs570891647	20:3,451,817	G/A	—	likely benign
rs2514328689	20:3,451,822	C/T	—	uncertain significance
rs773764349	20:3,451,835	C/T	—	likely benign
rs2084413488	20:3,451,836	G/T	—	uncertain significance
rs1238109620	20:3,451,847	G/C	—	uncertain significance
rs2084413851	20:3,451,851	T/C	—	uncertain significance
rs1002500321	20:3,451,889	C/G	—	likely benign
rs990180230	20:3,451,891	G/A	—	uncertain significance
rs1257568633	20:3,451,899	C/T	—	uncertain significance
rs6051882	20:3,451,908	C/T	—	benign
rs2084416122	20:3,451,930	C/A	—	uncertain significance
rs987494226	20:3,451,931	A/C	—	likely benign
rs2514329585	20:3,451,940	G/A	—	likely benign
rs567423892	20:3,451,950	T/C	—	benign
rs1363808562	20:3,451,958	C/G	—	likely benign
rs2084416894	20:3,451,960	C/G	—	uncertain significance
rs1188881494	20:3,451,980	C/T	—	likely benign
rs931076756	20:3,452,000	G/A	—	likely benign
rs866726262	20:3,452,001	G/A	—	uncertain significance
rs542464289	20:3,452,014	C/T	—	uncertain significance
rs762116548	20:3,452,018	G/A	—	likely benign
rs2146046226	20:3,452,033	A/T	—	likely benign
rs75653676	20:3,452,041	C/T	—	benign
rs2084419897	20:3,452,044	A/G	—	uncertain significance
rs879691653	20:3,452,047	C/T	—	uncertain significance
rs1219198471	20:3,452,102	C/T	—	uncertain significance
rs375793861	20:3,452,132	C/T	—	likely benign
rs2514330902	20:3,452,133	G/C	—	uncertain significance
rs778370767	20:3,452,138	A/G	—	likely benign
rs997964888	20:3,452,140	G/A	—	uncertain significance
rs771706436	20:3,452,150	C/G	—	uncertain significance
rs564825443	20:3,452,153	G/A	—	likely benign
rs777336042	20:3,452,156	C/T	—	likely benign
rs2146046656	20:3,452,162	C/A	—	uncertain significance
rs759497948	20:3,452,183	C/T	—	likely benign
rs117452972	20:3,454,201	C/T	intron variant	—
rs554125541	20:3,455,136	C/T	—	—
rs550587022	20:3,512,913	A/G	—	—
rs151518	20:3,515,924	G/A	—	benign
rs151519	20:3,515,951	C/T	—	benign
rs375750291	20:3,515,957	G/A	—	likely benign
rs1199796049	20:3,515,965	C/T	—	uncertain significance
rs1286559450	20:3,515,966	G/A	—	likely benign
rs932890371	20:3,515,980	G/T	—	uncertain significance
rs139505141	20:3,515,983	A/T	—	likely benign
rs571884856	20:3,516,275	T/C	—	—
rs6139149	20:3,518,137	G/T	intron variant	—
rs376960261	20:3,520,861	C/A	—	likely benign
rs2085598426	20:3,520,865	T/C	—	likely benign
rs759749245	20:3,520,871	C/A	—	uncertain significance
rs535151003	20:3,520,892	G/A	—	uncertain significance
rs2146189445	20:3,520,911	A/C	—	likely benign
rs2146189489	20:3,520,942	G/A	—	uncertain significance
rs780643690	20:3,520,944	T/G	—	uncertain significance
rs374983614	20:3,520,954	A/G	—	uncertain significance
rs140624366	20:3,526,415	C/T	—	likely benign
rs148044221	20:3,526,438	A/G	—	uncertain significance
rs763240659	20:3,526,441	A/G	—	uncertain significance
rs1423859127	20:3,526,443	A/G	—	uncertain significance
rs949307502	20:3,526,459	T/C	—	uncertain significance
rs564569898	20:3,526,526	T/C	—	likely benign
rs766199118	20:3,526,531	C/T	—	uncertain significance
rs547519747	20:3,526,542	G/C	—	uncertain significance
rs1481560758	20:3,527,948	A/G	—	uncertain significance
rs1290090939	20:3,527,974	A/C	—	uncertain significance
rs748613292	20:3,527,980	A/C	—	uncertain significance
rs369774374	20:3,527,991	C/T	—	likely benign
rs141713516	20:3,527,996	C/G	—	likely benign
rs2514494234	20:3,527,998	G/A	—	uncertain significance
rs373231195	20:3,528,007	G/A	—	uncertain significance
rs2146201683	20:3,528,034	G/A	—	uncertain significance
rs1231058647	20:3,528,046	C/T	—	uncertain significance
rs748332214	20:3,528,063	C/T	—	likely benign
rs2085721000	20:3,528,077	A/T	—	uncertain significance
rs1466163945	20:3,528,080	G/A	—	uncertain significance
rs138628890	20:3,528,092	A/C	—	uncertain significance
rs2514494559	20:3,528,095	C/T	—	uncertain significance
rs376268737	20:3,528,098	G/A	—	uncertain significance
rs6107308	20:3,528,101	A/C	—	benign
rs1351449101	20:3,528,114	C/T	—	likely benign
rs199516815	20:3,528,135	G/A	—	uncertain significance
rs954030033	20:3,529,825	T/C	—	uncertain significance
rs2146204126	20:3,529,833	T/A	—	likely benign
rs377163365	20:3,529,892	C/G	—	uncertain significance
rs756629370	20:3,529,917	C/T	—	likely benign
rs867467663	20:3,529,936	G/A	—	uncertain significance
rs778477025	20:3,529,939	G/A	—	uncertain significance
rs139431664	20:3,529,947	A/G	—	likely benign
rs147729396	20:3,529,952	T/C	—	uncertain significance
rs751796320	20:3,529,981	C/A	—	uncertain significance
rs201622481	20:3,529,993	G/A	—	likely benign
rs147164307	20:3,540,077	C/T	—	benign
rs997247524	20:3,540,078	G/T	—	uncertain significance
rs752682548	20:3,540,081	C/G	—	uncertain significance

Showing 100 of 310 variants. Use the SNP search for the full list.

Gene information from NCBI Gene. Variant classifications from ClinVar.