Variant (rsID / SNP)
rs143809043
rs143809043 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to PGAM2. Location: chromosome 7, position 44,104,567. Clinical significance in the table: Conflicting interpretations of pathogenicity.
Reference-table entries
PGAM2Conflicting interpretations
- Clinical significance (as recorded)
- Conflicting interpretations of pathogenicity
- Variant type
- single nucleotide variant
- Chromosome / position
- 7:44104567
- Cytoband
- 7p13
- HGVS
- NM_000290.4(PGAM2):c.459C>T (p.Cys153=)
- Allele change
- Synonymous_C153C
Associated conditions / phenotypes
Glycogen storage disease type X
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.