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VWA3B

von Willebrand factor A domain containing 3B

HCNC Approved Symbol
VWA3B (HGNC:28385)
Genomic Coordinates
2:98,087,167 - 98,330,616 (2q11.2)
Synonyms
DKFZp686F2227, MGC26733
Disease Associations
This gene is associated with the following 1 diseases in OMIM.

Diagnosed Cases

0Patient

There are no patients diagnosed with a variant in the VWA3B gene.

Frequently observed phenotypes

(Top 5 only, Patient count*)
*% of total patients presenting each phenotype is shown in parentheses.

No Results
VWA3B - Gene browser | 3billion