Variant (rsID / SNP)

rs10246939

rs10246939 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to TAS2R38. Location: chromosome 7, position 141,672,604. Clinical significance in the table: drug response.

ShareE-Mail WhatsApp LinkedIn X Facebook Telegram

Reference-table entries

TAS2R38Drug response

Clinical significance (as recorded): drug response
Variant type: single nucleotide variant
Chromosome / position: 7:141672604
Cytoband: 7q34
HGVS: NM_176817.5(TAS2R38):c.886A>G (p.Ile296Val)
Allele change: Missense_I296V

Associated conditions / phenotypes

Phenylthiocarbamide tasting

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.