rs146886371

This variant is located in the SNX29 gene.

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ClinVar annotation

Uncertain Significance★★★☆
3 submitters1 publication

not specified; not provided; Acute myeloid leukemia

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About SNX29

Predicted to enable phosphatidylinositol binding activity. [provided by Alliance of Genome Resources, Jul 2025]

View all SNX29 variants →

Gene information from NCBI Gene. Variant classifications from ClinVar.

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