rs376177936
This variant is located in the POMGNT2 gene.
▶ClinVar annotation
Uncertain Significance★★★☆
3 submitters1 publicationMuscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type a, 8; Inborn genetic diseases; not provided
View on ClinVar →About POMGNT2
This gene encodes a protein with glycosyltransferase activity although its function is not currently known. [provided by RefSeq, Sep 2012]
View all POMGNT2 variants →Gene information from NCBI Gene. Variant classifications from ClinVar.
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