IER5L

immediate early response 5 like

Known Variants29 total

rsid	Position (GRCh37)	Alleles	Class	ClinVar
rs1075650	9:131,938,913	T/C	coding sequence variant	—
rs1181292315	9:131,939,193	G/T	—	uncertain significance
rs776936905	9:131,939,199	G/A	—	uncertain significance
rs1176648199	9:131,939,371	G/C	—	uncertain significance
rs774228318	9:131,939,373	C/T	—	likely benign
rs761064660	9:131,939,390	G/C	—	uncertain significance
rs1829416815	9:131,939,430	T/G	—	uncertain significance
rs543581354	9:131,939,485	G/A	—	uncertain significance
rs761469519	9:131,939,545	C/T	—	uncertain significance
rs60193826	9:131,939,552	G/A	—	benign
rs765030656	9:131,939,584	A/C	—	uncertain significance
rs1200714445	9:131,939,586	T/C	—	uncertain significance
rs758715053	9:131,939,587	G/A	—	uncertain significance
rs780396725	9:131,939,604	G/A	—	uncertain significance
rs756707438	9:131,939,634	G/T	—	uncertain significance
rs192335853	9:131,939,651	C/A	—	benign
rs762772717	9:131,939,667	G/T	—	uncertain significance
rs1376977229	9:131,939,697	G/C	—	uncertain significance
rs1346187258	9:131,939,709	C/T	—	uncertain significance
rs1342415124	9:131,939,793	G/A	—	uncertain significance
rs912492285	9:131,939,803	G/A	—	uncertain significance
rs1039370891	9:131,939,820	C/A	—	uncertain significance
rs1829431909	9:131,939,848	G/A	—	uncertain significance
rs1454247935	9:131,939,937	G/A	—	uncertain significance
rs987974792	9:131,939,938	G/A	—	uncertain significance
rs184457	9:131,940,019	G/A	missense variant	—
rs1829441807	9:131,940,306	C/T	—	uncertain significance
rs375938981	9:131,940,322	C/T	—	uncertain significance
rs56784286	9:131,940,708	C/G	—	—

Gene information from NCBI Gene. Variant classifications from ClinVar.