rs143943051

This variant is located in the MAJIN gene.

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ClinVar annotation

Uncertain Significance★☆☆☆

2 submitters

not specified; Thyroid cancer, nonmedullary, 1

About MAJIN

Predicted to enable DNA binding activity. Predicted to be involved in homologous chromosome pairing at meiosis and meiotic attachment of telomere to nuclear envelope. Predicted to act upstream of or within double-strand break repair involved in meiotic recombination; oogenesis; and spermatogenesis. Predicted to be located in chromosome, telomeric region. Predicted to be active in nuclear inner membrane. [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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