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Variant (rsID / SNP)

rs11647490

PDIA2

rs11647490 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to PDIA2. Location: chromosome 16, position 336,660. The table records no clinical significance for this variant.

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Reference-table entries

PDIA2Not classified
Variant type
synonymous_variant
Chromosome / position
16:336660
HGVS
NM_006849.4,c.1347G>A,p.Thr449Thr
Allele change
Synonymous_T449T

Public references

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