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Variant (rsID / SNP)

rs144229867

PYGM

rs144229867 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to PYGM. Location: chromosome 11, position 64,514,740. Clinical significance in the table: Conflicting interpretations of pathogenicity.

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Reference-table entries

PYGMConflicting interpretations
Clinical significance (as recorded)
Conflicting interpretations of pathogenicity
Variant type
single nucleotide variant
Chromosome / position
11:64514740
Cytoband
11q13.1
HGVS
NM_005609.4(PYGM):c.2268C>T (p.Pro756=)
Allele change
Synonymous_P756P

Associated conditions / phenotypes

Glycogen storage disease, type V

Public references

Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.