Variant (rsID / SNP)

rs12226919

rs12226919 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to TAS2R20, PRH1. Location: chromosome 12, position 11,150,033. The table records no clinical significance for this variant.

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Reference-table entries

TAS2R20Not classified

Variant type: missense_variant
Chromosome / position: 12:11150033
HGVS: NM_176889.4,c.442C>A,p.His148Asn
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.