Variant (rsID / SNP)

rs1015443

rs1015443 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to TAS2R13, PRH1. Location: chromosome 12, position 11,061,122. The table records no clinical significance for this variant.

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Reference-table entries

TAS2R13Not classified

Variant type: missense_variant
Chromosome / position: 12:11061122
HGVS: NM_023920.2,c.776A>G,p.Asn259Ser
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.