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Variant (rsID / SNP)

rs149003893

PLK4

rs149003893 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to PLK4. Location: chromosome 4, position 128,802,306. Clinical significance in the table: Conflicting interpretations of pathogenicity.

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Reference-table entries

PLK4Conflicting interpretations
Clinical significance (as recorded)
Conflicting interpretations of pathogenicity
Variant type
single nucleotide variant
Chromosome / position
4:128802306
Cytoband
4q28.1
HGVS
NM_014264.5(PLK4):c.17G>A (p.Gly6Glu)
Allele change
Missense_G6E

Public references

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