Variant (rsID / SNP)

rs1726866

rs1726866 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to TAS2R38. Location: chromosome 7, position 141,672,705. Clinical significance in the table: Benign.

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Reference-table entries

TAS2R38Benign

Clinical significance (as recorded): Benign
Variant type: single nucleotide variant
Chromosome / position: 7:141672705
Cytoband: 7q34
HGVS: NM_176817.5(TAS2R38):c.785= (p.Ala262=)
Allele change: Missense_A262V

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.