Variant (rsID / SNP)

rs846664

rs846664 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to TAS2R16. Location: chromosome 7, position 122,635,173. Clinical significance in the table: Affects; risk factor.

ShareE-Mail WhatsApp LinkedIn X Facebook Telegram

Reference-table entries

TAS2R16Risk factor

Clinical significance (as recorded): Affects; risk factor
Variant type: single nucleotide variant
Chromosome / position: 7:122635173
Cytoband: 7q31.32
HGVS: NM_016945.3(TAS2R16):c.516T>G (p.Asn172Lys)
Allele change: Missense_N172K

Associated conditions / phenotypes

BETA-GLUCOPYRANOSIDE TASTING|Alcohol dependence, susceptibility to

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.