rs139278158

This variant is located in the NINL gene.

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ClinVar annotation

Likely Benign

2 submitters

NINL-related disorder; Melanoma; Hepatocellular carcinoma; Malignant tumor of esophagus

About NINL

Predicted to enable calcium ion binding activity. Predicted to be involved in microtubule anchoring at centrosome. Located in centrosome. [provided by Alliance of Genome Resources, Jul 2025]

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Gene information from NCBI Gene. Variant classifications from ClinVar.

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