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Variant (rsID / SNP)

rs45459806

PDIA2

rs45459806 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to PDIA2. Location: chromosome 16, position 335,531. The table records no clinical significance for this variant.

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Reference-table entries

PDIA2Not classified
Variant type
missense_variant
Chromosome / position
16:335531
HGVS
NM_006849.4,c.947C>T,p.Ala316Val
Allele change
Missense_A316V

Public references

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