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Gene entry

SGCD

sarcoglycan delta

Chromosome
5
Cytoband
5q33.2-q33.3
Variants (rsID)
210

SGCD is a protein-coding gene, meaning the body reads it as instructions to build a protein, located on chromosome 5 (region 5q33.2-q33.3). Its official name is “sarcoglycan delta”. The reference table lists 210 variants (rsID) for this gene.

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Clinically classified variants

14 reference-table entries with clinical significance.

  • rs3913482Benignsingle nucleotide variantLimb-Girdle Muscular Dystrophy, Recessive|Qualitative or quantitative defects of delta-sarcoglycan
  • rs45559835Benignsingle nucleotide variantQualitative or quantitative defects of delta-sarcoglycan|Limb-Girdle Muscular Dystrophy, Recessive|Autosomal recessive limb-girdle muscular dystrophy type 2F|Cardiovascular phenotype
  • rs180898690Conflicting interpretationssingle nucleotide variantDilated cardiomyopathy 1L|Autosomal recessive limb-girdle muscular dystrophy type 2F|Autosomal recessive limb-girdle muscular dystrophy type 2F
  • rs190935424Conflicting interpretationssingle nucleotide variantCardiovascular phenotype|Cardiomyopathy|Autosomal recessive limb-girdle muscular dystrophy type 2F
  • rs200451694Conflicting interpretationssingle nucleotide variantAutosomal recessive limb-girdle muscular dystrophy type 2F
  • rs200670993Conflicting interpretationssingle nucleotide variantAutosomal recessive limb-girdle muscular dystrophy type 2F|Qualitative or quantitative defects of delta-sarcoglycan
  • rs367819390Conflicting interpretationssingle nucleotide variantAutosomal recessive limb-girdle muscular dystrophy type 2F|Dilated cardiomyopathy 1L|Autosomal recessive limb-girdle muscular dystrophy type 2F
  • rs374043017Conflicting interpretationssingle nucleotide variantLimb-Girdle Muscular Dystrophy, Recessive|Qualitative or quantitative defects of delta-sarcoglycan
  • rs397516338Conflicting interpretationssingle nucleotide variantQualitative or quantitative defects of delta-sarcoglycan|Limb-Girdle Muscular Dystrophy, Recessive|Hypertrophic cardiomyopathy 1|Autosomal recessive limb-girdle muscular dystrophy type 2F|Primary dilated cardiomyopathy
  • rs397517923Conflicting interpretationssingle nucleotide variantDilated cardiomyopathy 1L|Autosomal recessive limb-girdle muscular dystrophy type 2F|Autosomal recessive limb-girdle muscular dystrophy type 2F
  • rs74846539Conflicting interpretationssingle nucleotide variantLimb-Girdle Muscular Dystrophy, Recessive|Qualitative or quantitative defects of delta-sarcoglycan|Cardiomyopathy|Autosomal recessive limb-girdle muscular dystrophy type 2F
  • rs121909296Pathogenicsingle nucleotide variantAutosomal recessive limb-girdle muscular dystrophy type 2F
  • rs121909298Uncertain significancesingle nucleotide variantDilated cardiomyopathy 1L|Autosomal recessive limb-girdle muscular dystrophy type 2F|MUSCULAR DYSTROPHY, LIMB-GIRDLE, AUTOSOMAL RECESSIVE 6, DIGENIC
  • rs376780156Uncertain significancesingle nucleotide variantAutosomal recessive limb-girdle muscular dystrophy type 2F

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.