LRRC56

leucine rich repeat containing 56

Summary

Predicted to be involved in cell projection organization. Predicted to be located in cilium. Implicated in primary ciliary dyskinesia 39. [provided by Alliance of Genome Resources, Jul 2025]

Known Variants299 total

rsidPosition (GRCh37)AllelesClassClinVar
rs37557463711:529,670A/G—benign
rs1124617811:540,584G/A—benign
rs7994846311:540,604A/C—benign
rs14296713911:540,709C/A—uncertain significance
rs77856604611:540,710G/A—uncertain significance
rs75835532011:540,718C/T—uncertain significance
rs227726911:540,719G/A—benign
rs76993246911:540,722G/A—uncertain significance
rs77252535011:540,736G/A—conflicting classifications of pathogenicity
rs57633076711:540,739C/T—uncertain significance
rs14452557011:540,740G/A—benign
rs253984760911:540,755G/A—uncertain significance
rs75219057411:540,756C/T—likely benign
rs77780495811:540,764G/T—uncertain significance
rs185175615211:540,766C/G—uncertain significance
rs76460161511:540,768G/T—likely benign
rs20069473711:540,777C/T—likely benign
rs253984800611:540,781C/G—uncertain significance
rs77374489411:540,782C/T—uncertain significance
rs76108610411:540,783A/T—likely benign
rs77138867911:540,788G/A—uncertain significance
rs253984815311:540,789C/T—likely benign
rs37453139811:540,795C/T—likely benign
rs105631131511:540,809G/A—uncertain significance
rs253984877711:540,843C/A—pathogenic
rs138554770611:540,844C/T—likely benign
rs37292207611:540,850C/T—uncertain significance
rs75521343711:540,856C/T—uncertain significance
rs102244729111:540,857G/A—uncertain significance
rs11468958111:540,865A/G—uncertain significance
rs185176256011:540,872G/A—likely benign
rs130905844311:540,873C/T—likely benign
rs77220317711:540,874G/A—likely benign
rs7284121911:541,462T/C—benign
rs37232556711:541,522G/C—likely benign
rs76617778811:541,549C/T—uncertain significance
rs14390886411:541,550G/A—uncertain significance
rs14728474411:541,561C/T—uncertain significance
rs14299560411:541,565G/A—benign
rs74962046911:541,577C/T—uncertain significance
rs77846737511:541,578G/A—likely benign
rs11686692611:541,601G/C—uncertain significance
rs19159247811:541,643C/T—benign
rs74647601711:541,644G/A—likely benign
rs6003851811:544,528G/T—benign
rs36787775911:544,708G/C—likely benign
rs76853929611:544,725C/T—uncertain significance
rs76096147811:544,736C/T—likely benign
rs77670327611:544,740G/A—uncertain significance
rs253987526411:544,745A/G—likely benign
rs77134066611:544,754G/C—likely benign
rs75312699011:544,757C/T—likely benign
rs76443787311:544,760C/T—likely benign
rs14458737811:544,770G/A—uncertain significance
rs78007973111:544,777T/C—uncertain significance
rs74917458211:544,779A/T—uncertain significance
rs156480085911:544,781G/A—pathogenic
rs37509979111:544,786C/T—uncertain significance
rs77422797511:544,787G/A—likely benign
rs185198951111:544,791G/A—likely benign
rs20040932211:544,793G/A—likely benign
rs37351694411:544,794G/C—likely benign
rs37667261311:544,799T/A—likely benign
rs7653766611:544,827C/T—benign
rs76220549811:549,888C/T—likely benign
rs253990544211:549,889C/T—likely benign
rs185228428811:549,895T/C—likely benign
rs36769330611:549,914G/A—likely benign
rs213405856111:549,921G/A—uncertain significance
rs75828446211:549,933G/A—uncertain significance
rs77741847611:549,935G/A—likely benign
rs74611576511:549,938G/A—likely benign
rs6174744711:549,946C/T—benign
rs37113594911:549,949G/A—uncertain significance
rs6174745011:549,957C/G—benign
rs794203011:549,959C/T—benign
rs11380835311:549,960G/A—conflicting classifications of pathogenicity
rs75352254311:549,978G/A—uncertain significance
rs75916087811:549,980C/T—likely benign
rs75274425311:549,986G/A—likely benign
rs156480503911:549,994T/C—pathogenic
rs156480505311:549,999G/A—pathogenic
rs76395515011:550,001G/C—uncertain significance
rs37576852911:550,013C/T—likely benign
rs1124618011:550,028G/C—benign
rs20034949411:550,058C/T—likely benign
rs75922835311:550,061G/A—likely benign
rs36936825411:550,062C/T—likely benign
rs20109114711:550,063G/A—likely benign
rs75262762811:550,079A/G—uncertain significance
rs14085213011:550,080C/T—likely benign
rs14324851311:550,081G/A—uncertain significance
rs144789239011:550,087T/G—uncertain significance
rs253990768511:550,090A/C—uncertain significance
rs57632617811:550,098C/A—likely benign
rs56084472111:550,100C/T—uncertain significance
rs36902311011:550,101G/C—likely benign
rs253990802011:550,125G/A—likely benign
rs148994957911:550,140G/C—likely benign
rs185230719011:550,142T/C—conflicting classifications of pathogenicity

Showing 100 of 299 variants. Use the SNP search for the full list.

Gene information from NCBI Gene. Variant classifications from ClinVar.