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Variant (rsID / SNP)

rs1128982

PKP3

rs1128982 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to PKP3. Location: chromosome 11, position 400,040. The table records no clinical significance for this variant.

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Reference-table entries

PKP3Not classified
Variant type
synonymous_variant
Chromosome / position
11:400040
HGVS
NM_001303029.2,c.1392A>G,p.Thr464Thr
Allele change
Synonymous_T464T

Public references

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