HEATR9

HEAT repeat containing 9

Summary

Predicted to act upstream of or within hematopoietic progenitor cell differentiation; response to cytokine; and response to virus. [provided by Alliance of Genome Resources, Jul 2025]

Known Variants33 total

rsidPosition (GRCh37)AllelesClassClinVar
rs77865093317:34,182,122G/A—uncertain significance
rs147885498017:34,182,127T/C—uncertain significance
rs214386381617:34,182,128A/G—likely benign
rs14197728817:34,182,149C/T—likely benign
rs37757587217:34,182,177C/G—uncertain significance
rs77070845517:34,182,194C/T—likely benign
rs75681241017:34,182,305T/C—uncertain significance
rs76658368317:34,182,393A/G—uncertain significance
rs75559366817:34,182,716C/A—uncertain significance
rs14359051717:34,182,733G/A—uncertain significance
rs14590369517:34,183,185T/C—uncertain significance
rs13872104617:34,183,195C/G—uncertain significance
rs77096729417:34,183,200G/A—uncertain significance
rs254420040517:34,183,802C/T—uncertain significance
rs7865584817:34,183,956G/C——
rs208784934717:34,185,294C/G—uncertain significance
rs254420922817:34,185,310G/A—uncertain significance
rs14634944317:34,185,899C/T—likely benign
rs74866249717:34,185,987C/T—uncertain significance
rs119482288317:34,190,012A/G—uncertain significance
rs254424147817:34,190,082C/T—uncertain significance
rs75898774217:34,190,105C/A—uncertain significance
rs254424178717:34,190,119A/C—uncertain significance
rs145615871017:34,190,542C/G—uncertain significance
rs208811261217:34,191,252C/T—uncertain significance
rs229129917:34,191,406T/G——
rs131510898917:34,191,782G/T—uncertain significance
rs11619123317:34,191,815G/A—not provided
rs14220688317:34,191,841C/T—uncertain significance
rs131698124217:34,192,256C/T—uncertain significance
rs14872867117:34,192,369T/C—uncertain significance
rs20066009917:34,192,378G/C—uncertain significance
rs479611917:34,193,088T/Cregulatory region variant—

Gene information from NCBI Gene. Variant classifications from ClinVar.