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Gene entry

FERMT1

FERM domain containing kindlin 1

Chromosome
20
Cytoband
20p12.3
Variants (rsID)
21

FERMT1 is a protein-coding gene, meaning the body reads it as instructions to build a protein, located on chromosome 20 (region 20p12.3). Its official name is “FERM domain containing kindlin 1”. The reference table lists 21 variants (rsID) for this gene.

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Clinically classified variants

7 reference-table entries with clinical significance.

  • rs1056141Benignsingle nucleotide variantKindler syndrome
  • rs16991866Benignsingle nucleotide variantKindler syndrome
  • rs2295435Benignsingle nucleotide variantKindler syndrome
  • rs6053878Benignsingle nucleotide variantKindler syndrome
  • rs62200482Benignsingle nucleotide variantKindler syndrome
  • rs753927Benignsingle nucleotide variantKindler syndrome
  • rs146180696Pathogenicsingle nucleotide variantKindler syndrome

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.