LAYN

layilin

Summary

Enables hyaluronic acid binding activity. Located in focal adhesion. [provided by Alliance of Genome Resources, Jul 2025]

Known Variants29 total

rsid	Position (GRCh37)	Alleles	Class	ClinVar
rs1290458062	11:111,411,603	T/G	—	uncertain significance
rs11213935	11:111,411,608	G/A	missense variant	benign
rs747772910	11:111,411,627	G/A	—	uncertain significance
rs189473926	11:111,412,284	C/T	—	benign
rs2497782445	11:111,414,692	G/A	—	uncertain significance
rs1867596955	11:111,414,729	T/G	—	uncertain significance
rs11827718	11:111,414,734	G/A	—	benign
rs146459063	11:111,414,869	C/T	—	uncertain significance
rs199956904	11:111,414,870	G/A	—	uncertain significance
rs770176909	11:111,420,392	A/T	—	uncertain significance
rs150283266	11:111,420,422	A/G	—	uncertain significance
rs1867709024	11:111,420,432	C/T	—	uncertain significance
rs760454342	11:111,420,459	G/A	—	uncertain significance
rs518294	11:111,424,716	A/T	intron variant	—
rs751005703	11:111,425,950	C/A	—	uncertain significance
rs748781024	11:111,425,988	G/A	—	uncertain significance
rs143930736	11:111,428,328	G/A	—	uncertain significance
rs773587902	11:111,430,824	C/T	—	uncertain significance
rs144227332	11:111,430,839	C/T	—	uncertain significance
rs2497814156	11:111,430,861	C/G	—	uncertain significance
rs368038262	11:111,430,863	A/G	—	uncertain significance
rs2497814483	11:111,430,914	G/A	—	uncertain significance
rs2497814578	11:111,430,951	C/T	—	uncertain significance
rs573383457	11:111,430,953	C/T	—	uncertain significance
rs114394665	11:111,431,050	C/T	—	benign
rs2497815106	11:111,431,056	G/A	—	uncertain significance
rs778966047	11:111,431,079	G/A	—	likely benign
rs1011699168	11:111,431,143	A/G	—	uncertain significance
rs542275	11:111,431,614	C/T	3 prime UTR variant	—

Gene information from NCBI Gene. Variant classifications from ClinVar.