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Variant (rsID / SNP)

rs1135029

PDE2A

rs1135029 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to PDE2A. Location: chromosome 11, position 72,289,291. The table records no clinical significance for this variant.

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Reference-table entries

PDE2ANot classified
Variant type
synonymous_variant
Chromosome / position
11:72289291
HGVS
NM_002599.5,c.2601A>G,p.Ala867Ala
Allele change
Synonymous_A867A

Public references

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