FOCAD

focadhesin

Summary

Predicted to be involved in regulation of post-transcriptional gene silencing. Located in cytosol and focal adhesion. [provided by Alliance of Genome Resources, Jul 2025]

Known Variants376 total

rsid	Position (GRCh37)	Alleles	Class	ClinVar
rs529838259	9:20,658,089	A/C	—	—
rs80214940	9:20,663,039	A/G	intron variant	—
rs73436459	9:20,715,277	G/T	—	benign
rs56301631	9:20,715,312	T/C	—	benign
rs1825246386	9:20,715,372	A/T	—	uncertain significance
rs201120976	9:20,715,401	C/A	—	uncertain significance
rs141452536	9:20,715,403	A/G	—	likely benign
rs1314305915	9:20,717,794	C/G	—	uncertain significance
rs772489765	9:20,717,857	C/A	—	uncertain significance
rs1472501871	9:20,720,367	G/A	—	likely benign
rs868300665	9:20,720,369	T/G	—	likely benign
rs775374663	9:20,720,388	T/C	—	likely benign
rs764916026	9:20,720,422	A/G	—	uncertain significance
rs2489181131	9:20,720,440	C/T	—	uncertain significance
rs2489181411	9:20,720,466	G/A	—	uncertain significance
rs1269880344	9:20,720,505	G/A	—	uncertain significance
rs4977898	9:20,720,599	A/C	—	benign
rs4446809	9:20,739,882	A/C	—	—
rs10115318	9:20,740,077	A/G	—	benign
rs144428211	9:20,740,264	T/C	—	uncertain significance
rs148407192	9:20,740,266	C/T	—	conflicting classifications of pathogenicity
rs1445934162	9:20,740,268	C/G	—	uncertain significance
rs142542466	9:20,740,272	C/A	—	uncertain significance
rs139972395	9:20,740,317	A/G	—	uncertain significance
rs373907768	9:20,740,321	A/G	—	uncertain significance
rs149760366	9:20,740,323	A/G	—	conflicting classifications of pathogenicity
rs17685673	9:20,740,433	A/T	—	benign
rs768062466	9:20,758,076	C/T	—	likely benign
rs773859024	9:20,758,078	G/T	—	likely benign
rs143814736	9:20,758,097	C/T	—	uncertain significance
rs141466501	9:20,758,183	C/A	—	uncertain significance
rs376024522	9:20,758,187	A/G	—	uncertain significance
rs369338363	9:20,758,197	T/C	—	uncertain significance
rs7851363	9:20,758,306	T/A	—	benign
rs10511687	9:20,764,870	C/T	—	benign
rs1829920184	9:20,764,883	C/T	—	likely benign
rs531535960	9:20,764,896	G/T	—	uncertain significance
rs2489783092	9:20,764,899	C/A	—	uncertain significance
rs149130519	9:20,764,916	G/C	—	likely benign
rs957948486	9:20,764,918	A/G	—	uncertain significance
rs148930782	9:20,764,928	A/G	—	likely benign
rs200873740	9:20,764,956	C/T	—	pathogenic
rs758744690	9:20,765,017	C/T	—	uncertain significance
rs7871811	9:20,765,097	G/A	—	benign
rs62557526	9:20,765,205	A/G	—	benign
rs73438327	9:20,769,822	C/T	—	benign
rs7860490	9:20,769,987	T/G	—	benign
rs10441706	9:20,770,031	G/A	—	benign
rs141572748	9:20,770,050	C/T	—	conflicting classifications of pathogenicity
rs141558162	9:20,770,059	C/T	—	conflicting classifications of pathogenicity
rs747948304	9:20,770,061	A/G	—	uncertain significance
rs762151102	9:20,770,097	C/T	—	uncertain significance
rs2489901822	9:20,770,104	C/G	—	uncertain significance
rs201808793	9:20,770,113	G/A	—	uncertain significance
rs758140968	9:20,770,136	A/T	—	uncertain significance
rs2489903717	9:20,770,162	A/T	—	uncertain significance
rs200516182	9:20,770,235	G/A	—	uncertain significance
rs1818062832	9:20,770,238	G/A	—	uncertain significance
rs186635487	9:20,770,257	A/T	—	benign
rs116067246	9:20,778,489	C/T	—	benign
rs77036953	9:20,778,514	C/T	—	benign
rs76546645	9:20,778,526	T/G	—	benign
rs7875153	9:20,778,631	A/G	intron variant	benign
rs145736340	9:20,778,661	T/C	—	benign
rs747741968	9:20,778,664	C/T	—	likely benign
rs767334883	9:20,778,705	T/C	—	uncertain significance
rs750263830	9:20,778,708	G/A	—	uncertain significance
rs747833477	9:20,778,721	A/G	—	likely benign
rs7849260	9:20,779,004	A/G	—	benign
rs4977729	9:20,779,006	G/A	—	benign
rs142574510	9:20,781,718	A/G	—	benign
rs752676826	9:20,781,734	C/A	—	uncertain significance
rs752730916	9:20,781,782	C/T	—	uncertain significance
rs759470768	9:20,781,808	A/G	—	uncertain significance
rs144110783	9:20,781,827	G/A	—	conflicting classifications of pathogenicity
rs1001970680	9:20,781,855	C/T	—	uncertain significance
rs147163830	9:20,781,859	T/C	—	likely benign
rs140435235	9:20,781,868	G/T	—	conflicting classifications of pathogenicity
rs148691031	9:20,781,902	G/A	—	uncertain significance
rs7038826	9:20,781,922	C/T	—	benign
rs2490099493	9:20,781,924	A/G	—	uncertain significance
rs746124907	9:20,781,942	C/G	—	likely benign
rs6475473	9:20,781,979	A/C	—	benign
rs7027599	9:20,782,100	T/C	—	benign
rs10964700	9:20,789,159	A/T	—	benign
rs74707685	9:20,789,231	T/A	—	benign
rs375080683	9:20,789,335	G/A	—	likely benign
rs2490226096	9:20,789,349	G/C	—	uncertain significance
rs142646886	9:20,789,378	C/A	—	likely benign
rs375010349	9:20,789,384	T/C	—	uncertain significance
rs75184203	9:20,789,424	A/G	—	benign
rs936391143	9:20,789,448	T/C	—	uncertain significance
rs2490228368	9:20,789,485	A/G	—	uncertain significance
rs150412472	9:20,789,502	G/A	—	likely benign
rs772501625	9:20,789,521	G/T	—	uncertain significance
rs2490229230	9:20,789,540	A/G	—	uncertain significance
rs112541381	9:20,789,545	G/A	—	likely benign
rs78653020	9:20,789,546	G/C	—	benign
rs765559875	9:20,789,552	A/G	—	uncertain significance
rs35908843	9:20,789,568	C/T	—	benign

Showing 100 of 376 variants. Use the SNP search for the full list.

Gene information from NCBI Gene. Variant classifications from ClinVar.