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Variant (rsID / SNP)

rs139882066

GBE1

rs139882066 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to GBE1. Location: chromosome 3, position 81,720,013. Clinical significance in the table: Benign/Likely benign.

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Reference-table entries

GBE1Benign
Clinical significance (as recorded)
Benign/Likely benign
Variant type
single nucleotide variant
Chromosome / position
3:81720013
Cytoband
3p12.2
HGVS
NM_000158.4(GBE1):c.405C>T (p.Leu135=)
Allele change
Synonymous_L135L

Associated conditions / phenotypes

Adult polyglucosan body disease|Glycogen storage disease, type IV|Glycogen storage disease, type IV|Glycogen storage disease IV, classic hepatic

Public references

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