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Gene entry

WIPF1

WAS/WASL interacting protein family member 1

Chromosome
2
Cytoband
2q31.1
Variants (rsID)
22

WIPF1 is a protein-coding gene, meaning the body reads it as instructions to build a protein, located on chromosome 2 (region 2q31.1). Its official name is “WAS/WASL interacting protein family member 1”. The reference table lists 22 variants (rsID) for this gene.

Clinically classified variants

1 reference-table entries with clinical significance.

  • rs4972450Benignsingle nucleotide variantWiskott-Aldrich syndrome 2

Other listed variants

Public references

Data from the institutional reference table and public NCBI annotation. For education only; not a substitute for medical or genetic counselling.