Variant (rsID / SNP)

rs62621450

rs62621450 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to TET2, TET2-AS1. Location: chromosome 4, position 106,197,000. The table records no clinical significance for this variant.

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Reference-table entries

TET2Not classified

Variant type: single nucleotide variant
Chromosome / position: 4:106197000
Cytoband: 4q24
HGVS: NM_001127208.3(TET2):c.5333A>G (p.His1778Arg)
Allele change: Missense_H1778R

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.