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Gene entry

TRPM4

transient receptor potential cation channel subfamily M member 4

Chromosome
19
Cytoband
19q13.33
Variants (rsID)
31

TRPM4 is a protein-coding gene, meaning the body reads it as instructions to build a protein, located on chromosome 19 (region 19q13.33). Its official name is “transient receptor potential cation channel subfamily M member 4”. The reference table lists 31 variants (rsID) for this gene.

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Clinically classified variants

13 reference-table entries with clinical significance.

  • rs113984787Benignsingle nucleotide variantProgressive familial heart block type IB|Cardiovascular phenotype
  • rs138603244Benignsingle nucleotide variantProgressive familial heart block type IB|Cardiovascular phenotype
  • rs3745301Benignsingle nucleotide variantProgressive familial heart block type IB|Cardiovascular phenotype
  • rs56355369Benignsingle nucleotide variantVentricular fibrillation|Cardiovascular phenotype|Arrhythmogenic right ventricular cardiomyopathy|Cardiomyopathy|Progressive familial heart block type IB
  • rs78444754Benignsingle nucleotide variantProgressive familial heart block type IB
  • rs140799936Conflicting interpretationssingle nucleotide variantTRPM4-Related Disorders|Cardiomyopathy|Progressive familial heart block type IB
  • rs144781529Conflicting interpretationssingle nucleotide variantCardiovascular phenotype|Progressive familial heart block type IB
  • rs145771389Conflicting interpretationssingle nucleotide variantProgressive familial heart block type IB
  • rs148855956Conflicting interpretationssingle nucleotide variantProgressive familial heart block type IB|Cardiomyopathy
  • rs200633475Conflicting interpretationssingle nucleotide variantProgressive familial heart block type IB
  • rs56118173Conflicting interpretationssingle nucleotide variantCardiovascular phenotype|Progressive familial heart block type IB
  • rs142312281Likely benignsingle nucleotide variantProgressive familial heart block type IB|7 conditions
  • rs200132598Uncertain significancesingle nucleotide variantProgressive familial heart block type IB

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.