Variant (rsID / SNP)

rs2842899

rs2842899 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to TAAR9. Location: chromosome 6, position 132,859,609. The table records no clinical significance for this variant.

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Reference-table entries

TAAR9Not classified

Variant type: stop_lost
Chromosome / position: 6:132859609
HGVS: NM_175057.4,c.181T>A,p.Ter61Lysext*?
Allele change: Missense_X61K

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.