PDE2A

phosphodiesterase 2A

Summary

Enables several functions, including 3',5'-cyclic-nucleotide phosphodiesterase activity; anion binding activity; and metal ion binding activity. Involved in several processes, including cellular response to cytokine stimulus; regulation of signal transduction; and regulation of vascular permeability. Located in several cellular components, including cytosol; mitochondrial membrane; and perinuclear region of cytoplasm. [provided by Alliance of Genome Resources, Jul 2025]

Known Variants267 total

rsidPosition (GRCh37)AllelesClassClinVar
rs14427957111:72,288,431C/T—likely benign
rs213526319311:72,288,434A/G—likely benign
rs14296717111:72,288,437A/T—benign
rs134329349111:72,288,459A/T—uncertain significance
rs75476081511:72,288,463G/A—uncertain significance
rs56797975211:72,288,497C/T—likely benign
rs76454425111:72,288,518C/T—likely benign
rs142896927211:72,288,525T/C—uncertain significance
rs127822355311:72,288,540C/A—uncertain significance
rs76704041911:72,288,541G/A—uncertain significance
rs14108236911:72,288,548G/A—likely benign
rs75376159111:72,288,566G/T—likely benign
rs77882628211:72,288,575C/T—likely benign
rs145859039811:72,288,579C/T—uncertain significance
rs198009111:72,288,599G/A—benign
rs249621876711:72,288,606T/A—uncertain significance
rs57803224911:72,288,611C/T—likely benign
rs75451386411:72,288,651G/C—benign
rs249622439611:72,289,263A/G—likely benign
rs128009737311:72,289,285G/A—likely benign
rs113502911:72,289,291C/T—benign
rs77096047211:72,289,342C/A—likely benign
rs77910517511:72,289,360C/T—likely benign
rs77133280311:72,289,394C/T—likely benign
rs78011830511:72,289,399C/T—likely benign
rs77500947511:72,289,400G/A—likely benign
rs249622668711:72,289,501G/A—likely benign
rs185556472311:72,289,511C/T—likely benign
rs249622682611:72,289,513C/T—likely benign
rs77442200311:72,289,571C/G—likely benign
rs36909945011:72,289,934C/G—benign
rs126397693711:72,289,941C/T—uncertain significance
rs249623083911:72,289,966C/A—uncertain significance
rs129963041511:72,290,001G/A—likely benign
rs105297959711:72,290,007G/A—likely benign
rs75473954611:72,290,041C/T—uncertain significance
rs77393755511:72,290,045C/T—uncertain significance
rs14105543111:72,290,046G/A—likely benign
rs77330220111:72,290,062G/A—likely benign
rs37324790611:72,290,066G/A—likely benign
rs36767060111:72,290,322A/G—uncertain significance
rs77174922611:72,290,360C/T—uncertain significance
rs20003232911:72,290,361G/A—uncertain significance
rs14503625411:72,290,407A/G—likely benign
rs121753709511:72,290,434C/T—likely benign
rs20223846911:72,290,444G/A—likely benign
rs116434730711:72,290,565C/A—likely benign
rs92576283211:72,290,571C/T—likely benign
rs148807296511:72,290,596A/C—uncertain significance
rs36812704211:72,290,601T/C—uncertain significance
rs213526996411:72,290,606C/T—uncertain significance
rs37236676511:72,290,611G/A—likely benign
rs39256511:72,290,629A/G—benign
rs19250931011:72,290,656G/C—conflicting classifications of pathogenicity
rs76575603411:72,290,671T/C—likely benign
rs77351764211:72,291,608A/C—likely benign
rs74703224411:72,291,630G/A—uncertain significance
rs140245581411:72,291,648G/A—likely benign
rs14688177611:72,291,651C/T—likely benign
rs11165717711:72,291,670T/C—likely pathogenic
rs249624892911:72,291,686A/G—likely benign
rs135892053611:72,291,914C/T—likely benign
rs57479098411:72,291,923G/A—likely benign
rs57753611:72,291,927T/C—benign
rs142532833511:72,291,931G/A—uncertain significance
rs134288006911:72,291,987G/A—likely benign
rs159101208711:72,291,996C/T—likely benign
rs140413143611:72,291,998A/G—likely benign
rs14629960911:72,292,005G/T—likely benign
rs76911089411:72,292,024G/T—likely benign
rs11629008111:72,292,032G/A—benign
rs77003122811:72,292,408A/C—uncertain significance
rs20178278311:72,292,466G/A—likely benign
rs37448271311:72,292,506T/C—uncertain significance
rs36936358611:72,292,527G/T—likely benign
rs185573933211:72,292,916C/T—pathogenic
rs74673167911:72,292,917G/A—uncertain significance
rs77057644311:72,292,921C/T—uncertain significance
rs37494921511:72,292,929G/A—likely benign
rs147046730411:72,292,950G/A—likely benign
rs141439634011:72,293,485C/T—uncertain significance
rs11746801211:72,293,490T/C—uncertain significance
rs11660468011:72,293,494C/T—likely benign
rs249626734711:72,293,543T/C—uncertain significance
rs75765778911:72,293,554G/A—likely benign
rs213527885011:72,293,585A/G—uncertain significance
rs494455711:72,293,602A/G—benign
rs77691030611:72,293,605G/A—likely benign
rs75272542711:72,293,613A/G—uncertain significance
rs76054369011:72,294,462G/C—likely benign
rs76986726011:72,294,469C/G—likely benign
rs13829149511:72,294,533C/T—likely benign
rs249627484711:72,294,573G/A—likely benign
rs117372299911:72,295,233C/A—likely benign
rs11677600211:72,295,341G/C—benign
rs213528451111:72,295,349C/G—uncertain significance
rs249628341511:72,295,350G/C—uncertain significance
rs249628343411:72,295,358C/T—uncertain significance
rs185585840011:72,295,372G/A—likely benign
rs19991848011:72,295,583C/T—benign

Showing 100 of 267 variants. Use the SNP search for the full list.

Gene information from NCBI Gene. Variant classifications from ClinVar.