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Gene entry

CSRP3

cysteine and glycine rich protein 3

Chromosome
11
Cytoband
11p15.1
Variants (rsID)
24

CSRP3 is a protein-coding gene, meaning the body reads it as instructions to build a protein, located on chromosome 11 (region 11p15.1). Its official name is “cysteine and glycine rich protein 3”. The reference table lists 24 variants (rsID) for this gene.

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Clinically classified variants

10 reference-table entries with clinical significance.

  • rs45476991Benignsingle nucleotide variantDilated cardiomyopathy 1M|Hypertrophic cardiomyopathy 12|Cardiovascular phenotype|Hypertrophic cardiomyopathy 12|Cardiomyopathy
  • rs104894205Conflicting interpretationssingle nucleotide variantHypertrophic cardiomyopathy 12|Cardiovascular phenotype|Dilated cardiomyopathy 1M|Hypertrophic cardiomyopathy 12|Hypertrophic cardiomyopathy
  • rs138218523Conflicting interpretationssingle nucleotide variantHypertrophic cardiomyopathy|Cardiovascular phenotype|Dilated cardiomyopathy 1M|Hypertrophic cardiomyopathy 12|Hypertrophic cardiomyopathy 12|Cardiomyopathy
  • rs142019584Conflicting interpretationssingle nucleotide variantHypertrophic cardiomyopathy 12|Hypertrophic cardiomyopathy 12|Dilated cardiomyopathy 1M
  • rs185980145Conflicting interpretationssingle nucleotide variantPrimary familial hypertrophic cardiomyopathy|Cardiomyopathy|Hypertrophic cardiomyopathy 12|Dilated cardiomyopathy 1M
  • rs193922667Conflicting interpretationssingle nucleotide variantCardiomyopathy|Dilated cardiomyopathy 1M|Hypertrophic cardiomyopathy 12
  • rs45498797Conflicting interpretationssingle nucleotide variantHypertrophic cardiomyopathy 12|Cardiomyopathy
  • rs45550635Conflicting interpretationssingle nucleotide variantDilated cardiomyopathy 1M|Primary dilated cardiomyopathy|Hypertrophic cardiomyopathy 12|Cardiovascular phenotype|Cardiomyopathy|Hypertrophic cardiomyopathy|Sudden unexplained death|Hypertrophic cardiomyopathy 12|Dilated cardiomyopathy 1M
  • rs137852764Uncertain significancesingle nucleotide variantDilated cardiomyopathy 1M|Dilated cardiomyopathy 1M|Hypertrophic cardiomyopathy 12|Cardiovascular phenotype|Hypertrophic cardiomyopathy
  • rs137852765Uncertain significancesingle nucleotide variantHypertrophic cardiomyopathy 12|Dilated cardiomyopathy 1M|Hypertrophic cardiomyopathy 12|Cardiomyopathy

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.