Variant (rsID / SNP)

rs28730706

rs28730706 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to AGL. Location: chromosome 1, position 100,377,973. Clinical significance in the table: Benign.

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Reference-table entries

AGLBenign

Clinical significance (as recorded): Benign
Variant type: single nucleotide variant
Chromosome / position: 1:100377973
Cytoband: 1p21.2
HGVS: NM_000642.3(AGL):c.3849T>C (p.Ala1283=)
Allele change: Synonymous_A1283A

Associated conditions / phenotypes

Glycogen storage disease type III

Public references

dbSNP
ClinVar
Ensembl
gnomAD

Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.