TMEM94

transmembrane protein 94

Summary

Enables P-type magnesium transporter activity. Involved in magnesium ion transport from cytosol to endoplasmic reticulum. Is active in endoplasmic reticulum membrane. [provided by Alliance of Genome Resources, Jul 2025]

Known Variants141 total

rsidPosition (GRCh37)AllelesClassClinVar
rs54866480817:73,481,542C/T—uncertain significance
rs75397255717:73,481,621C/T—uncertain significance
rs14209401817:73,481,638C/T—likely benign
rs75567095917:73,482,011G/A—likely benign
rs55428197917:73,482,036G/A—uncertain significance
rs14128210017:73,482,060G/A—benign
rs75998771717:73,482,075G/A—uncertain significance
rs37637609617:73,482,085C/T—likely benign
rs14334932817:73,482,373G/T—uncertain significance
rs15128943617:73,482,397C/T—uncertain significance
rs126558385817:73,482,417C/T—uncertain significance
rs76221843817:73,482,420C/T—uncertain significance
rs56345158917:73,482,450C/T—uncertain significance
rs14344841817:73,482,463G/C—uncertain significance
rs37587333517:73,482,474C/T—uncertain significance
rs37051472817:73,482,475G/A—uncertain significance
rs139215013917:73,484,062A/G—likely benign
rs76154307317:73,484,090T/C—uncertain significance
rs14490550217:73,484,834C/T—uncertain significance
rs13856716517:73,484,845C/T—likely benign
rs14926100617:73,484,846G/A—uncertain significance
rs36968785617:73,484,883C/G—uncertain significance
rs75713569017:73,484,907G/C—uncertain significance
rs15059716817:73,484,957C/T—uncertain significance
rs135201037317:73,485,346G/C—pathogenic
rs11538916117:73,485,353C/G—uncertain significance
rs159840058717:73,485,358A/G—uncertain significance
rs75488422317:73,485,399C/T—uncertain significance
rs54663800617:73,485,441G/A—uncertain significance
rs14605038417:73,485,681C/T—likely benign
rs205196056617:73,485,715C/T—uncertain significance
rs19392106817:73,485,742A/G—uncertain significance
rs254586519417:73,486,313A/G—likely pathogenic
rs75782006817:73,486,390C/T—uncertain significance
rs77121537917:73,486,414G/T—uncertain significance
rs14576001717:73,486,801G/T—uncertain significance
rs76229103317:73,486,843C/A—likely benign
rs14899170617:73,487,137T/C—uncertain significance
rs19984294317:73,487,164G/A—uncertain significance
rs56745629717:73,487,167T/G—uncertain significance
rs11242569017:73,487,183G/A—likely benign
rs127574306917:73,487,218G/A—uncertain significance
rs75622482617:73,487,441A/G—uncertain significance
rs77035101217:73,487,773C/T—uncertain significance
rs3570991817:73,487,830A/G—benign
rs205220984617:73,487,835C/T—pathogenic
rs56544882017:73,487,842G/A—likely benign
rs37295505217:73,487,899C/T—uncertain significance
rs205222079917:73,487,929C/T—uncertain significance
rs14599190817:73,487,934G/A—uncertain significance
rs205229689217:73,488,558C/T—pathogenic
rs7489468617:73,488,576G/A—uncertain significance
rs89089901817:73,488,577A/C—uncertain significance
rs146506936917:73,488,599T/A—uncertain significance
rs14606121717:73,488,630C/T—uncertain significance
rs205230729117:73,488,679A/G—uncertain significance
rs37086572217:73,488,760G/T—uncertain significance
rs77507169317:73,488,776C/T—likely benign
rs407825917:73,488,794T/C—benign
rs121661284617:73,488,813A/G—uncertain significance
rs14770869617:73,488,816G/A—likely benign
rs37443625617:73,488,819G/A—uncertain significance
rs36865861817:73,488,855C/T—uncertain significance
rs121771042617:73,489,129C/T—uncertain significance
rs76196890917:73,489,130G/A—uncertain significance
rs75047968017:73,489,135C/G—uncertain significance
rs14041491717:73,489,215C/Gupstream gene variant—
rs407847417:73,489,567G/C—benign
rs74677313117:73,489,593A/G—uncertain significance
rs98024492917:73,489,798C/G—uncertain significance
rs74613111217:73,489,805C/T—pathogenic
rs14883248217:73,489,813C/T—likely benign
rs53770415117:73,489,909C/T—likely benign
rs156796727617:73,489,923T/C—uncertain significance
rs77709869017:73,489,953T/C—uncertain significance
rs14162119917:73,489,958A/G—likely benign
rs20020900417:73,489,970G/A—likely benign
rs14174340517:73,489,974G/A—likely benign
rs37544871917:73,489,976C/T—uncertain significance
rs36897706917:73,490,771T/C—uncertain significance
rs254598326917:73,490,780T/C—uncertain significance
rs20153564117:73,490,816G/A—uncertain significance
rs101929518617:73,490,848C/T—uncertain significance
rs104036762917:73,490,883A/G—likely benign
rs125120121817:73,491,058G/A—uncertain significance
rs78059591717:73,491,063C/G—uncertain significance
rs36857886717:73,491,068C/A—uncertain significance
rs37503911317:73,491,085G/A—uncertain significance
rs77696558217:73,491,114G/C—uncertain significance
rs18217387117:73,491,360C/T—likely benign
rs214683196417:73,491,363A/G—pathogenic
rs55774650617:73,491,370C/T—pathogenic
rs137093754417:73,491,371G/A—uncertain significance
rs95005760417:73,491,396C/G—likely benign
rs36937056917:73,491,408G/A—likely benign
rs75580650417:73,491,416C/T—uncertain significance
rs14727127317:73,491,441G/A—likely benign
rs254600367317:73,491,476A/G—uncertain significance
rs14796371117:73,491,630G/A—likely benign
rs77622496617:73,491,643A/G—uncertain significance

Showing 100 of 141 variants. Use the SNP search for the full list.

Gene information from NCBI Gene. Variant classifications from ClinVar.