rs767711936
This variant is located in the MYCN gene.
▶ClinVar annotation
About MYCN
This gene is a member of the MYC family and encodes a protein with a basic helix-loop-helix (bHLH) domain. This protein is located in the nucleus and must dimerize with another bHLH protein in order to bind DNA. Amplification of this gene is associated with a variety of tumors, most notably neuroblastomas. Multiple alternatively spliced transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jun 2014]
View all MYCN variants →Gene information from NCBI Gene. Variant classifications from ClinVar.
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