Variant (rsID / SNP)

rs2842934

rs2842934 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to TPMT. Location: chromosome 6, position 18,139,214. Clinical significance in the table: Likely benign.

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Reference-table entries

TPMTLikely benign

Clinical significance (as recorded): Likely benign
Variant type: single nucleotide variant
Chromosome / position: 6:18139214
Cytoband: 6p22.3
HGVS: NM_000367.5(TPMT):c.474C>T (p.Ile158=)
Allele change: Synonymous_I158I

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.