Variant (rsID / SNP)

rs112384084

rs112384084 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to TNK2. Location: chromosome 3, position 195,594,494. Clinical significance in the table: Conflicting interpretations of pathogenicity.

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Reference-table entries

TNK2Conflicting interpretations

Clinical significance (as recorded): Conflicting interpretations of pathogenicity
Variant type: single nucleotide variant
Chromosome / position: 3:195594494
Cytoband: 3q29
HGVS: NM_001382273.1(TNK2):c.2675G>A (p.Arg892His)
Allele change: Missense_R909H

Associated conditions / phenotypes

Parkinson disease

Public references

dbSNP
ClinVar
Ensembl
gnomAD

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