LRRC36

leucine rich repeat containing 36

Known Variants33 total

rsid	Position (GRCh37)	Alleles	Class	ClinVar
rs149543891	16:67,367,735	C/G	intron variant	—
rs756071408	16:67,375,863	T/C	—	uncertain significance
rs1318140834	16:67,375,866	T/G	—	uncertain significance
rs7184253	16:67,380,550	T/C	regulatory region variant	—
rs1184415767	16:67,381,412	C/A	—	uncertain significance
rs766587513	16:67,381,469	A/G	—	uncertain significance
rs367748415	16:67,384,179	G/A	—	likely benign
rs1471143	16:67,386,349	C/G	intron variant	—
rs756830733	16:67,397,513	A/C	—	uncertain significance
rs9922085	16:67,397,580	G/A	missense variant	—
rs1597480449	16:67,399,219	G/A	—	uncertain significance
rs774350561	16:67,400,935	C/T	—	uncertain significance
rs140418859	16:67,400,959	C/T	—	uncertain significance
rs762633681	16:67,401,321	C/A	—	uncertain significance
rs1597484656	16:67,401,337	G/A	—	uncertain significance
rs761329204	16:67,404,897	G/A	—	uncertain significance
rs144677421	16:67,404,942	C/T	—	uncertain significance
rs2039616160	16:67,404,972	G/A	—	uncertain significance
rs779977479	16:67,404,985	C/T	—	uncertain significance
rs138358333	16:67,404,994	G/C	—	uncertain significance
rs200059387	16:67,409,157	C/T	—	uncertain significance
rs8052655	16:67,409,180	G/A	missense variant	—
rs749805396	16:67,409,249	C/T	—	uncertain significance
rs111417813	16:67,410,666	C/T	—	uncertain significance
rs2508407311	16:67,410,726	G/A	—	uncertain significance
rs764672675	16:67,410,774	T/C	—	uncertain significance
rs750526016	16:67,412,513	G/C	—	uncertain significance
rs2508427936	16:67,412,576	G/C	—	uncertain significance
rs142444346	16:67,415,083	C/T	intron variant	—
rs768189219	16:67,416,039	A/T	—	uncertain significance
rs1053752377	16:67,416,072	A/G	—	uncertain significance
rs2508473046	16:67,418,814	A/G	—	uncertain significance
rs2040239603	16:67,418,816	A/G	—	uncertain significance

Gene information from NCBI Gene. Variant classifications from ClinVar.