Variant (rsID / SNP)

rs144386291

rs144386291 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to TET2. Location: chromosome 4, position 106,157,698. Clinical significance in the table: Benign.

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Reference-table entries

TET2Benign

Clinical significance (as recorded): Benign
Variant type: single nucleotide variant
Chromosome / position: 4:106157698
Cytoband: 4q24
HGVS: NM_001127208.3(TET2):c.2599T>C (p.Tyr867His)
Allele change: Missense_Y867H

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.