Variant (rsID / SNP)

rs307377

rs307377 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to TAS1R3. Location: chromosome 1, position 1,269,554. The table records no clinical significance for this variant.

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Reference-table entries

TAS1R3Not classified

Variant type: missense_variant
Chromosome / position: 1:1269554
HGVS: NM_152228.3,c.2269T>C,p.Cys757Arg
Allele change: Missense_C757R

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.