Variant (rsID / SNP)

rs111948941

rs111948941 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to TET2, TET2-AS1. Location: chromosome 4, position 106,155,199. 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: 4:106155199
Cytoband: 4q24
HGVS: NM_001127208.3(TET2):c.100C>T (p.Leu34Phe)
Allele change: Missense_L34F

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.