Variant (rsID / SNP)

rs139716296

rs139716296 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to PMM2. Location: chromosome 16, position 8,898,702. Clinical significance in the table: Pathogenic.

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Reference-table entries

PMM2Pathogenic

Clinical significance (as recorded): Pathogenic
Variant type: single nucleotide variant
Chromosome / position: 16:8898702
Cytoband: 16p13.2
HGVS: NM_000303.3(PMM2):c.255+2T>C
Allele change: Silent

Associated conditions / phenotypes

PMM2-congenital disorder of glycosylation|Intellectual disability

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.