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Variant (rsID / SNP)

rs2074739

PLA2G3

rs2074739 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to PLA2G3. Location: chromosome 22, position 31,533,967. The table records no clinical significance for this variant.

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Reference-table entries

PLA2G3Not classified
Variant type
synonymous_variant
Chromosome / position
22:31533967
HGVS
NM_015715.5,c.795C>T,p.Tyr265Tyr
Allele change
Synonymous_Y265Y

Public references

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