rs1833994284

This variant is located in the WDR37 gene.

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ClinVar annotation

Conflicting Classifications
3 submitters1 publication

Neurooculocardiogenitourinary syndrome; not provided

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About WDR37

This gene encodes a member of the WD repeat protein family. WD repeats are minimally conserved regions of approximately 40 amino acids typically bracketed by gly-his and trp-asp (GH-WD), which may facilitate formation of heterotrimeric or multiprotein complexes. Members of this family are involved in a variety of cellular processes, including cell cycle progression, signal transduction, apoptosis, and gene regulation. [provided by RefSeq, Jul 2008]

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Gene information from NCBI Gene. Variant classifications from ClinVar.

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