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Variant (rsID / SNP)

rs137852891

GBE1

rs137852891 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to GBE1. Location: chromosome 3, position 81,584,397. Clinical significance in the table: Conflicting interpretations of pathogenicity.

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Reference-table entries

GBE1Conflicting interpretations
Clinical significance (as recorded)
Conflicting interpretations of pathogenicity
Variant type
single nucleotide variant
Chromosome / position
3:81584397
Cytoband
3p12.2
HGVS
NM_000158.4(GBE1):c.1883A>G (p.His628Arg)
Allele change
Missense_H628R

Associated conditions / phenotypes

Glycogen storage disease due to glycogen branching enzyme deficiency, childhood neuromuscular form|Glycogen storage disease, type IV|Glycogen storage disease IV, classic hepatic|Glycogen storage disease, type IV

Public references

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