Variant (rsID / SNP)

rs1126690

rs1126690 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to GAA. Location: chromosome 17, position 78,091,405. Clinical significance in the table: Benign.

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Reference-table entries

GAABenign

Clinical significance (as recorded): Benign
Variant type: single nucleotide variant
Chromosome / position: 17:78091405
Cytoband: 17q25.3
HGVS: NM_000152.5(GAA):c.2338G>A (p.Val780Ile)
Allele change: Missense_V780I

Associated conditions / phenotypes

Glycogen storage disease, type II

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.