Variant (rsID / SNP)

rs115707514

rs115707514 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to TAS2R31, PRH1. Location: chromosome 12, position 11,183,506. The table records no clinical significance for this variant.

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Reference-table entries

TAS2R31Not classified

Variant type: missense_variant
Chromosome / position: 12:11183506
HGVS: NM_176885.2,c.429A>T,p.Gln143His
Allele change: Silent

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.