RFX7

regulatory factor X7

Summary

RFX7 is a member of the regulatory factor X (RFX) family of transcription factors (see RFX1, MIM 600006) (Aftab et al., 2008 [PubMed 18673564]).[supplied by OMIM, Mar 2009]

Known Variants122 total

rsidPosition (GRCh37)AllelesClassClinVar
rs1697673415:56,382,295A/C——
rs250498407815:56,385,567A/C—uncertain significance
rs250498427815:56,385,658A/C—uncertain significance
rs36885516315:56,385,742T/C—likely benign
rs18339620715:56,385,775A/G—likely benign
rs250498471615:56,385,837C/G—uncertain significance
rs56872531515:56,385,859C/A—uncertain significance
rs37517704615:56,385,886T/C—likely benign
rs75379942015:56,385,910A/G—uncertain significance
rs74721996715:56,385,952T/G—uncertain significance
rs18893032915:56,385,955C/T—likely benign
rs250498511215:56,386,075G/A—uncertain significance
rs148285036415:56,386,138T/C—uncertain significance
rs20012121915:56,386,174T/C—likely benign
rs77018133815:56,386,175T/C—uncertain significance
rs54425839315:56,386,195G/A—uncertain significance
rs37379883715:56,386,357C/T—uncertain significance
rs19177327015:56,386,432C/T—likely benign
rs75450957215:56,386,433G/A—likely benign
rs11772439215:56,386,514T/A—benign
rs78164450115:56,386,529T/C—uncertain significance
rs77258510415:56,386,547C/G—uncertain significance
rs75957272415:56,386,567C/T—uncertain significance
rs717058915:56,386,577T/G—benign
rs78138868815:56,386,649G/A—uncertain significance
rs250498626815:56,386,679G/A—uncertain significance
rs77404128815:56,386,717C/G—uncertain significance
rs250498649215:56,386,771G/A—uncertain significance
rs250498712615:56,386,837C/A—uncertain significance
rs250498713715:56,386,843G/A—pathogenic
rs250498714615:56,386,844G/A—pathogenic
rs214051161915:56,386,858G/A—uncertain significance
rs250498743115:56,386,978C/G—uncertain significance
rs75696359015:56,386,996C/T—uncertain significance
rs214051192215:56,386,999G/C—uncertain significance
rs120560476215:56,387,005C/T—uncertain significance
rs250498750715:56,387,012A/T—uncertain significance
rs77946155415:56,387,034C/T—likely benign
rs3436172915:56,387,142G/A—benign
rs76953148515:56,387,153T/C—uncertain significance
rs75080178715:56,387,208G/T—pathogenic
rs129837963215:56,387,214A/T—uncertain significance
rs250498795715:56,387,222T/C—uncertain significance
rs19981134115:56,387,226C/A—likely benign
rs75442926015:56,387,239T/G—uncertain significance
rs78070578615:56,387,252C/T—likely benign
rs54937388915:56,387,337C/G—uncertain significance
rs77382795515:56,387,340C/G—uncertain significance
rs11752848115:56,387,352T/C—likely benign
rs76368017515:56,387,446G/A—uncertain significance
rs76491710915:56,387,458A/C—pathogenic
rs250498848015:56,387,516C/G—uncertain significance
rs18232184115:56,387,532T/C—benign
rs89575603915:56,387,542C/A—uncertain significance
rs18681459115:56,387,574T/C—likely benign
rs250498869115:56,387,633A/G—uncertain significance
rs250498878015:56,387,683G/C—uncertain significance
rs250498881215:56,387,693C/A—likely pathogenic
rs54033740615:56,387,750T/C—uncertain significance
rs214051373015:56,387,779C/G—uncertain significance
rs144929853015:56,387,810C/T—uncertain significance
rs77695534815:56,387,815T/C—uncertain significance
rs76532571715:56,387,828G/A—uncertain significance
rs250498909815:56,387,834T/C—uncertain significance
rs146053536415:56,387,855C/A—uncertain significance
rs54325242515:56,387,900T/C—likely benign
rs20148840415:56,387,960G/A—uncertain significance
rs250498939615:56,387,966T/C—uncertain significance
rs19995451015:56,387,972A/T—uncertain significance
rs56959022015:56,388,082G/A—likely benign
rs147053948415:56,388,083T/C—likely benign
rs37540429815:56,388,098G/C—uncertain significance
rs36946667515:56,388,113G/A—uncertain significance
rs250498976815:56,388,121C/T—uncertain significance
rs37699966115:56,388,205T/C—uncertain significance
rs1697675115:56,388,334C/T—uncertain significance
rs137559779615:56,388,340G/A—uncertain significance
rs250499047715:56,388,352C/G—uncertain significance
rs20118174315:56,388,356A/G—likely benign
rs54283887415:56,388,377C/T—likely benign
rs204167490815:56,388,401G/T—uncertain significance
rs129386992515:56,388,404C/T—likely benign
rs20196897415:56,388,407T/C—likely benign
rs78048537615:56,388,455G/C—uncertain significance
rs250499082315:56,388,461G/C—uncertain significance
rs75181087115:56,388,478C/T—likely benign
rs250499088315:56,388,482G/A—uncertain significance
rs75614128415:56,388,650G/A—uncertain significance
rs37387938715:56,388,668C/T—likely benign
rs37067066015:56,388,731T/A—uncertain significance
rs75948142615:56,388,761T/G—uncertain significance
rs54740802915:56,388,764C/T—likely benign
rs37550320915:56,388,779T/C—likely benign
rs74811036615:56,388,784C/T—likely benign
rs56948089415:56,388,805C/G—uncertain significance
rs20052941315:56,388,811C/T—likely benign
rs37379544415:56,390,309G/A—likely benign
rs250499402915:56,390,323G/A—uncertain significance
rs78142516815:56,390,421G/T—uncertain significance
rs75321703915:56,390,461G/A—likely benign

Showing 100 of 122 variants. Use the SNP search for the full list.

Gene information from NCBI Gene. Variant classifications from ClinVar.