Variant (rsID / SNP)

rs79011721

rs79011721 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to PGM1. Location: chromosome 1, position 64,095,975. Clinical significance in the table: Likely benign.

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Reference-table entries

PGM1Likely benign

Clinical significance (as recorded): Likely benign
Variant type: single nucleotide variant
Chromosome / position: 1:64095975
Cytoband: 1p31.3
HGVS: NM_002633.3(PGM1):c.556+216C>T
Allele change: Silent

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.