rs36044892
This variant is located in the TCN1 gene.
▶ClinVar annotation
Uncertain Significance★★★☆
3 submitters1 publicationnot provided; Transcobalamin I deficiency; not specified
View on ClinVar →About TCN1
This gene encodes a member of the vitamin B12-binding protein family. This family of proteins, alternatively referred to as R binders, is expressed in various tissues and secretions. This protein is a major constituent of secondary granules in neutrophils and facilitates the transport of cobalamin into cells. [provided by RefSeq, Jul 2008]
View all TCN1 variants →Gene information from NCBI Gene. Variant classifications from ClinVar.
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