Variant (rsID / SNP)

rs17602729

rs17602729 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to AMPD1. Location: chromosome 1, position 115,236,057. Clinical significance in the table: Conflicting interpretations of pathogenicity; other.

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Reference-table entries

AMPD1Conflicting interpretations

Clinical significance (as recorded): Conflicting interpretations of pathogenicity; other
Variant type: single nucleotide variant
Chromosome / position: 1:115236057
Cytoband: 1p13.2
HGVS: NM_000036.3(AMPD1):c.34C>T (p.Gln12Ter)
Allele change: Silent

Associated conditions / phenotypes

Muscle AMP deaminase deficiency

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.