rs370747546
This variant is located in the SH2B3 gene.
▶ClinVar annotation
not provided; not specified; Inborn genetic diseases
View on ClinVar →About SH2B3
This gene encodes a member of the SH2B adaptor family of proteins, which are involved in a range of signaling activities by growth factor and cytokine receptors. The encoded protein is a key negative regulator of cytokine signaling and plays a critical role in hematopoiesis. Mutations in this gene have been associated with susceptibility to celiac disease type 13 and susceptibility to insulin-dependent diabetes mellitus. Alternatively spliced transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Apr 2014]
View all SH2B3 variants →Gene information from NCBI Gene. Variant classifications from ClinVar.
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