Variant (rsID / SNP)

rs713598

rs713598 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to TAS2R38. Location: chromosome 7, position 141,673,345. Clinical significance in the table: drug response.

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Reference-table entries

TAS2R38Drug response

Clinical significance (as recorded): drug response
Variant type: single nucleotide variant
Chromosome / position: 7:141673345
Cytoband: 7q34
HGVS: NM_176817.5(TAS2R38):c.145G>C (p.Ala49Pro)
Allele change: Missense_A49P

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.