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Gene entry

SGCG

sarcoglycan gamma

Chromosome
13
Cytoband
13q12.12
Variants (rsID)
79

SGCG is a protein-coding gene, meaning the body reads it as instructions to build a protein, located on chromosome 13 (region 13q12.12). Its official name is “sarcoglycan gamma”. The reference table lists 79 variants (rsID) for this gene.

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Clinically classified variants

12 reference-table entries with clinical significance.

  • rs17314986Benignsingle nucleotide variantSevere autosomal recessive muscular dystrophy of childhood - North African type|Limb-Girdle Muscular Dystrophy, Recessive|Sarcoglycanopathy
  • rs1800351Benignsingle nucleotide variantLimb-Girdle Muscular Dystrophy, Recessive|Severe autosomal recessive muscular dystrophy of childhood - North African type|Sarcoglycanopathy
  • rs4770403Benignsingle nucleotide variantLimb-Girdle Muscular Dystrophy, Recessive|Sarcoglycanopathy
  • rs114160429Conflicting interpretationssingle nucleotide variantSevere autosomal recessive muscular dystrophy of childhood - North African type
  • rs139369964Conflicting interpretationssingle nucleotide variantLimb-Girdle Muscular Dystrophy, Recessive|Sarcoglycanopathy|Severe autosomal recessive muscular dystrophy of childhood - North African type
  • rs141771521Conflicting interpretationssingle nucleotide variantSarcoglycanopathy|Limb-Girdle Muscular Dystrophy, Recessive
  • rs199905729Conflicting interpretationssingle nucleotide variantSevere autosomal recessive muscular dystrophy of childhood - North African type
  • rs745599370Conflicting interpretationssingle nucleotide variant
  • rs104894422Pathogenicsingle nucleotide variantSevere autosomal recessive muscular dystrophy of childhood - North African type
  • rs104894423Pathogenicsingle nucleotide variantSevere autosomal recessive muscular dystrophy of childhood - North African type
  • rs762777463PathogenicDuplicationSevere autosomal recessive muscular dystrophy of childhood - North African type
  • rs148404730Uncertain significancesingle nucleotide variantSevere autosomal recessive muscular dystrophy of childhood - North African type

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.