rs766769136

This variant is located in the BNC2 gene.

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ClinVar annotation

Uncertain Significance★★★☆
2 submitters2 publications

not provided; Lower urinary tract obstruction, congenital

View on ClinVar →

About BNC2

This gene encodes a conserved zinc finger protein. The encoded protein functions in skin color saturation. Mutations in this gene are associated with facial pigmented spots. This gene is also associated with susceptibility to adolescent idiopathic scoliosis. [provided by RefSeq, Jul 2016]

View all BNC2 variants →

Gene information from NCBI Gene. Variant classifications from ClinVar.

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