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SCGB1C2

secretoglobin family 1C member 2

HCNC Approved Symbol
SCGB1C2 (HGNC:51242)
Genomic Coordinates
: - (17p13.3)
Synonyms
Disease Associations
Currently, this gene is not associated with any human disease in OMIM.

Diagnosed Cases

There are no diagnosed cases at this time.
There are no patients* with variants predicted to be damaging.* None of the patients have been diagnosed with a variant in another gene.

SCGB1C2 - Gene browser | 3billion