Variant (rsID / SNP)

rs56260729

rs56260729 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to TNK2. Location: chromosome 3, position 195,594,950. 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: 3:195594950
Cytoband: 3q29
HGVS: NM_001382273.1(TNK2):c.2219C>T (p.Pro740Leu)
Allele change: Missense_P757L

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.