Variant (rsID / SNP)

rs117474773

rs117474773 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to GYS2. Location: chromosome 12, position 21,689,946. Clinical significance in the table: Benign/Likely benign.

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Reference-table entries

GYS2Benign

Clinical significance (as recorded): Benign/Likely benign
Variant type: single nucleotide variant
Chromosome / position: 12:21689946
Cytoband: 12p12.1
HGVS: NM_021957.4(GYS2):c.2054T>C (p.Phe685Ser)
Allele change: Missense_F685S

Associated conditions / phenotypes

Glycogen storage disorder due to hepatic glycogen synthase deficiency

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.