Variant (rsID / SNP)

rs1669413

rs1669413 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to TAS2R42. Location: chromosome 12, position 11,338,781. The table records no clinical significance for this variant.

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Reference-table entries

TAS2R42Not classified

Variant type: missense_variant
Chromosome / position: 12:11338781
HGVS: NM_181429.2,c.763G>T,p.Gly255Trp
Allele change: Missense_G255W

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.