WNT2B

Wnt family member 2B

Summary

This gene encodes a member of the wingless-type MMTV integration site (WNT) family of highly conserved, secreted signaling factors. WNT family members function in a variety of developmental processes including regulation of cell growth and differentiation and are characterized by a WNT-core domain. This gene may play a role in human development as well as carcinogenesis. Alternative splicing results in multiple transcript variants. [provided by RefSeq, May 2014]

Known Variants128 total

rsidPosition (GRCh37)AllelesClassClinVar
rs120381191:113,043,423A/C——
rs1831148131:113,047,858T/Cupstream gene variant—
rs5367012091:113,051,634C/A——
rs7680854531:113,051,893A/G—likely benign
rs13149207601:113,051,895C/T—uncertain significance
rs13734778821:113,051,896G/C—likely benign
rs7740225921:113,051,897G/C—uncertain significance
rs10032815771:113,051,907A/C—uncertain significance
rs360066791:113,051,909A/G—benign
rs7463374221:113,051,919A/G—uncertain significance
rs10210429961:113,051,931G/C—uncertain significance
rs2018952251:113,051,933C/T—uncertain significance
rs38280751:113,051,936G/A—uncertain significance
rs12986456251:113,051,938C/G—likely benign
rs7631022901:113,051,946C/G—uncertain significance
rs7518552831:113,051,949T/C—uncertain significance
rs5642382321:113,051,951C/T—uncertain significance
rs7502162261:113,051,953T/C—likely benign
rs3744176051:113,051,957C/A—uncertain significance
rs3770643731:113,051,962G/A—likely benign
rs7478368391:113,051,963C/T—uncertain significance
rs1995229501:113,051,966G/A—conflicting classifications of pathogenicity
rs11949049701:113,051,974C/T—likely benign
rs11712927771:113,051,978G/C—uncertain significance
rs7635099951:113,051,986G/A—likely benign
rs9833878081:113,052,010C/G—likely benign
rs12639738991:113,052,034G/A—likely benign
rs7538605361:113,052,035A/G—uncertain significance
rs7548775981:113,052,037G/T—likely benign
rs25264762011:113,052,042C/G—uncertain significance
rs16522630221:113,052,044G/A—uncertain significance
rs14467648311:113,052,060C/G—uncertain significance
rs12678009271:113,052,081C/A—likely benign
rs5476454431:113,057,483C/T—likely benign
rs25264949271:113,057,507C/T—uncertain significance
rs25264949391:113,057,512G/T—uncertain significance
rs3773425801:113,057,514G/A—likely benign
rs3702441481:113,057,518C/T—likely pathogenic
rs7795915121:113,057,535T/C—likely benign
rs5339897131:113,057,538C/T—likely benign
rs7722412471:113,057,541T/C—likely benign
rs7767772141:113,057,555G/A—uncertain significance
rs7771935101:113,057,563C/T—pathogenic
rs7526562151:113,057,565G/C—uncertain significance
rs2016624501:113,057,602G/A—uncertain significance
rs5351675531:113,057,604C/T—likely benign
rs1404452061:113,057,615G/A—benign
rs8792554201:113,057,626C/T—uncertain significance
rs7779666961:113,057,627G/A—uncertain significance
rs11732152661:113,057,634T/C—likely benign
rs25264957151:113,057,637G/A—likely benign
rs13985993031:113,057,647C/T—uncertain significance
rs7709761491:113,057,664C/T—likely benign
rs25264958611:113,057,679C/T—likely benign
rs1450111151:113,057,681G/A—uncertain significance
rs7630189771:113,057,690C/G—uncertain significance
rs7742745331:113,057,700C/T—likely benign
rs3716223071:113,057,731C/T—likely benign
rs16525288221:113,058,756C/A—likely benign
rs7490376671:113,058,784A/G—likely benign
rs25264997481:113,058,791A/T—uncertain significance
rs1378555461:113,058,814C/T—likely benign
rs1504736351:113,058,815G/A—uncertain significance
rs1169236701:113,058,826C/T—likely benign
rs25265001021:113,058,862T/C—likely benign
rs7644988841:113,058,876G/A—uncertain significance
rs350585561:113,058,897G/A—uncertain significance
rs1427162771:113,058,909A/C—uncertain significance
rs1497162931:113,058,940C/T—likely benign
rs7508862901:113,058,959G/T—uncertain significance
rs9641434381:113,058,960C/T—uncertain significance
rs2009729871:113,058,961C/T—likely benign
rs7552214031:113,058,979G/T—uncertain significance
rs7706164761:113,058,999G/A—uncertain significance
rs7761775461:113,059,000G/A—likely benign
rs11999052341:113,059,003C/T—likely benign
rs7541428981:113,059,008T/C—uncertain significance
rs1808240401:113,059,026G/A—uncertain significance
rs7556957781:113,059,753G/A—uncertain significance
rs7490044411:113,059,780A/G—uncertain significance
rs16525930071:113,059,783G/A—conflicting classifications of pathogenicity
rs7784786701:113,059,784C/T—likely benign
rs1126385281:113,059,793T/C—benign
rs14478375051:113,059,806C/T—uncertain significance
rs25265063631:113,059,821G/A—uncertain significance
rs7757084711:113,059,840G/A—uncertain significance
rs7517680521:113,059,860C/T—pathogenic
rs7617029331:113,059,863C/T—uncertain significance
rs1410703011:113,059,877T/C—likely benign
rs7533576341:113,059,880G/A—likely benign
rs7544168861:113,059,883G/A—likely benign
rs3682727521:113,059,916C/T—likely benign
rs1502463301:113,059,917G/A—uncertain significance
rs12557534201:113,059,922C/A—likely benign
rs7604539811:113,059,938C/T—uncertain significance
rs10116911151:113,059,946C/T—likely benign
rs7524429671:113,059,949G/A—likely benign
rs13877871901:113,059,970C/T—likely benign
rs25265076851:113,059,975C/T—uncertain significance
rs14858594691:113,059,990T/A—uncertain significance

Showing 100 of 128 variants. Use the SNP search for the full list.

Gene information from NCBI Gene. Variant classifications from ClinVar.