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VWC2

von Willebrand factor C domain containing 2

HCNC Approved Symbol
VWC2 (HGNC:30200)
Genomic Coordinates
7:49,773,638 - 49,922,205 (7p12.2)
Synonyms
PSST739, UNQ739
Disease Associations
Currently, this gene is not associated with any human disease in OMIM.

Diagnosed Cases

There are no diagnosed cases at this time.
However, there are 4 patients* with variant(s) predicted to be damaging.*1 of the patient has been diagnosed with a variant in another gene.

VWC2 - Gene browser | 3billion