Variant (rsID / SNP)

rs72681118

rs72681118 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to PGM1. Location: chromosome 1, position 64,095,862. Clinical significance in the table: Benign.

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Reference-table entries

PGM1Benign

Clinical significance (as recorded): Benign
Variant type: single nucleotide variant
Chromosome / position: 1:64095862
Cytoband: 1p31.3
HGVS: NM_002633.3(PGM1):c.556+103G>A
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.