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Gene entry

PIGT

phosphatidylinositol glycan anchor biosynthesis class T

Chromosome
20
Cytoband
20q13.12
Variants (rsID)
8

PIGT is a protein-coding gene, meaning the body reads it as instructions to build a protein, located on chromosome 20 (region 20q13.12). Its official name is “phosphatidylinositol glycan anchor biosynthesis class T”. The reference table lists 8 variants (rsID) for this gene.

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Clinically classified variants

4 reference-table entries with clinical significance.

  • rs61753669Benignsingle nucleotide variantMultiple congenital anomalies-hypotonia-seizures syndrome 3
  • rs707577Benignsingle nucleotide variantMultiple congenital anomalies-hypotonia-seizures syndrome 3|Paroxysmal nocturnal hemoglobinuria 2
  • rs80158178Benignsingle nucleotide variantMultiple congenital anomalies-hypotonia-seizures syndrome 3
  • rs139366969Conflicting interpretationssingle nucleotide variantMultiple congenital anomalies-hypotonia-seizures syndrome 3

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.