Variant (rsID / SNP)

rs3747669

rs3747669 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to TNK2. Location: chromosome 3, position 195,615,376. Clinical significance in the table: Benign.

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Reference-table entries

TNK2Benign

Clinical significance (as recorded): Benign
Variant type: single nucleotide variant
Chromosome / position: 3:195615376
Cytoband: 3q29
HGVS: NM_001382273.1(TNK2):c.84T>C (p.Asp28=)
Allele change: Synonymous_D60D

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.