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Gene entry

SLC37A4

solute carrier family 37 member 4

Chromosome
11
Cytoband
11q23.3
Variants (rsID)
22

SLC37A4 is a protein-coding gene, meaning the body reads it as instructions to build a protein, located on chromosome 11 (region 11q23.3). Its official name is “solute carrier family 37 member 4”. The reference table lists 22 variants (rsID) for this gene.

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Clinically classified variants

16 reference-table entries with clinical significance.

  • rs34871377Benignsingle nucleotide variantGlucose-6-phosphate transport defect
  • rs35010541Benignsingle nucleotide variantGlucose-6-phosphate transport defect|Phosphate transport defect
  • rs61730035Benignsingle nucleotide variantGlucose-6-phosphate transport defect|Glycogen storage disease due to glucose-6-phosphatase deficiency type IA|Phosphate transport defect
  • rs121908976Conflicting interpretationssingle nucleotide variantPhosphate transport defect|Glucose-6-phosphate transport defect|Glycogen storage disease, type I
  • rs148971334Conflicting interpretationssingle nucleotide variantGlucose-6-phosphate transport defect
  • rs186476316Conflicting interpretationssingle nucleotide variantGlucose-6-phosphate transport defect|Phosphate transport defect|Glucose-6-phosphate transport defect
  • rs193302889Conflicting interpretationssingle nucleotide variantGlycogen storage disease, type I|6 conditions|Glucose-6-phosphate transport defect
  • rs193302887Likely pathogenicsingle nucleotide variantGlucose-6-phosphate transport defect
  • rs193302888Pathogenicsingle nucleotide variantGlucose-6-phosphate transport defect
  • rs781784543Pathogenicsingle nucleotide variantGlucose-6-phosphate transport defect
  • rs80356489Pathogenicsingle nucleotide variantGlucose-6-phosphate transport defect
  • rs80356490Pathogenicsingle nucleotide variantGlucose-6-phosphate transport defect
  • rs80356491PathogenicDeletionPhosphate transport defect|Glucose-6-phosphate transport defect|Inborn genetic diseases|Glycogen storage disease|Glucose-6-phosphate transport defect|Phosphate transport defect|Congenital disorder of glycosylation, type IIw
  • rs141105181Uncertain significancesingle nucleotide variantGlucose-6-phosphate transport defect
  • rs149974794Uncertain significancesingle nucleotide variantGlucose-6-phosphate transport defect
  • rs181879065Uncertain significancesingle nucleotide variantGlucose-6-phosphate transport defect

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.