FPR1

formyl peptide receptor 1

Summary

This gene encodes a G protein-coupled receptor of mammalian phagocytic cells that is a member of the G-protein coupled receptor 1 family. The protein mediates the response of phagocytic cells to invasion of the host by microorganisms and is important in host defense and inflammation.[provided by RefSeq, Jul 2010]

Known Variants198 total

rsidPosition (GRCh37)AllelesClassClinVar
rs15082062219:52,249,204C/T—likely benign
rs13948091619:52,249,210C/T—likely benign
rs86722819:52,249,211T/G—benign
rs123298213719:52,249,232G/A—uncertain significance
rs251391906919:52,249,233T/C—uncertain significance
rs77171366619:52,249,238T/C—uncertain significance
rs77502653519:52,249,240G/T—likely benign
rs1784997119:52,249,255A/G—benign
rs251391913019:52,249,266A/G—uncertain significance
rs55133852319:52,249,272C/T—uncertain significance
rs76815290119:52,249,273G/C—likely benign
rs212232066719:52,249,279G/A—likely benign
rs75091226619:52,249,288C/T—likely benign
rs37554123219:52,249,291A/G—likely benign
rs159980619319:52,249,293T/G—uncertain significance
rs76670044719:52,249,294G/C—likely benign
rs20140421219:52,249,296C/T—uncertain significance
rs14008344519:52,249,305C/T—uncertain significance
rs74915456019:52,249,306G/A—likely benign
rs208374137219:52,249,314G/A—likely benign
rs55569062319:52,249,322C/T—uncertain significance
rs208374151119:52,249,329C/T—uncertain significance
rs125374070919:52,249,330C/T—likely benign
rs118317148519:52,249,334C/A—uncertain significance
rs251391931519:52,249,346T/C—uncertain significance
rs76824172319:52,249,350G/C—uncertain significance
rs52949807519:52,249,351C/T—uncertain significance
rs251391942119:52,249,372G/A—likely benign
rs37169236419:52,249,390T/C—likely benign
rs90315505019:52,249,395C/T—uncertain significance
rs75721712019:52,249,397T/C—uncertain significance
rs251391951419:52,249,407T/C—uncertain significance
rs251391952919:52,249,419T/G—uncertain significance
rs155579636419:52,249,421T/C—uncertain significance
rs55373802019:52,249,422A/G—uncertain significance
rs74659368119:52,249,424A/G—uncertain significance
rs208374259719:52,249,425T/C—uncertain significance
rs54772511019:52,249,426G/A—benign
rs212232127419:52,249,427C/G—uncertain significance
rs14221001619:52,249,442C/T—benign
rs77144605119:52,249,443G/A—uncertain significance
rs146097896019:52,249,473C/T—uncertain significance
rs19392089619:52,249,476G/A—uncertain significance
rs212232148319:52,249,490C/A—uncertain significance
rs134586514319:52,249,496A/T—uncertain significance
rs76681894319:52,249,497A/G—uncertain significance
rs14557865719:52,249,504T/G—likely benign
rs76437005219:52,249,509C/T—uncertain significance
rs14889822019:52,249,510G/A—likely benign
rs208374345119:52,249,512C/A—uncertain significance
rs14358372719:52,249,522G/A—likely benign
rs57525519019:52,249,525C/A—likely benign
rs75283653519:52,249,526C/T—uncertain significance
rs14764692419:52,249,527G/A—uncertain significance
rs36807554119:52,249,535C/T—uncertain significance
rs130230922819:52,249,538C/T—uncertain significance
rs37152450119:52,249,541G/C—uncertain significance
rs159980646119:52,249,543C/T—likely benign
rs88929489419:52,249,552G/C—likely benign
rs119776090319:52,249,566T/A—uncertain significance
rs14191382819:52,249,574G/A—uncertain significance
rs119211930319:52,249,584C/T—uncertain significance
rs208374447119:52,249,594A/T—likely benign
rs14577581419:52,249,596C/A—uncertain significance
rs77582544019:52,249,600G/A—likely benign
rs37203782419:52,249,602T/C—uncertain significance
rs3526476519:52,249,603G/A—benign
rs251391995319:52,249,606C/T—uncertain significance
rs208374466119:52,249,607A/C—uncertain significance
rs14122991019:52,249,609G/A—likely benign
rs76516462319:52,249,614C/T—uncertain significance
rs208374487419:52,249,624A/G—likely benign
rs20046439319:52,249,625A/G—uncertain significance
rs251392000119:52,249,626T/A—uncertain significance
rs212232207019:52,249,630G/A—likely benign
rs148994504119:52,249,635G/A—uncertain significance
rs15023973319:52,249,641T/C—likely benign
rs74889340819:52,249,652G/A—uncertain significance
rs143139966119:52,249,657C/T—uncertain significance
rs251392009519:52,249,659T/C—uncertain significance
rs20188016219:52,249,665C/T—conflicting classifications of pathogenicity
rs74754080619:52,249,666G/A—likely benign
rs104222919:52,249,672A/Cmissense variantbenign
rs77316299719:52,249,678C/G—uncertain significance
rs503088019:52,249,680T/A—benign
rs36980568919:52,249,684T/C—likely benign
rs13976090419:52,249,689G/A—uncertain significance
rs57198777519:52,249,692C/T—uncertain significance
rs53989357319:52,249,693G/A—likely benign
rs251392021619:52,249,694T/C—uncertain significance
rs14597315919:52,249,695T/C—likely benign
rs251392023019:52,249,700C/T—uncertain significance
rs207074619:52,249,702T/G—benign
rs75332515819:52,249,705C/T—likely benign
rs14607516419:52,249,706G/A—uncertain significance
rs208374603619:52,249,707A/G—uncertain significance
rs74745034419:52,249,714A/T—uncertain significance
rs76922329419:52,249,720G/A—likely benign
rs78140081019:52,249,724G/A—uncertain significance
rs74861560219:52,249,729T/A—likely benign

Showing 100 of 198 variants. Use the SNP search for the full list.

Gene information from NCBI Gene. Variant classifications from ClinVar.