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Variant (rsID / SNP)

rs2289025

PARD3B

rs2289025 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to PARD3B. Location: chromosome 2, position 205,969,220. The table records no clinical significance for this variant.

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Reference-table entries

PARD3BNot classified
Variant type
missense_variant
Chromosome / position
2:205969220
HGVS
NM_001302769.2,c.575G>A,p.Arg192Lys
Allele change
Missense_R192K

Public references

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