Variant (rsID / SNP)

rs1548803

rs1548803 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to TAS2R8. Location: chromosome 12, position 10,959,031. The table records no clinical significance for this variant.

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Reference-table entries

TAS2R8Not classified

Variant type: synonymous_variant
Chromosome / position: 12:10959031
HGVS: NM_023918.3,c.549G>A,p.Leu183Leu
Allele change: Synonymous_L183L

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.