Variant (rsID / SNP)

rs1800888

rs1800888 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to ADRB2. Location: chromosome 5, position 148,206,885. Clinical significance in the table: drug response.

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Reference-table entries

ADRB2Drug response

Clinical significance (as recorded): drug response
Variant type: single nucleotide variant
Chromosome / position: 5:148206885
Cytoband: 5q32
HGVS: NM_000024.6(ADRB2):c.491C>T (p.Thr164Ile)
Allele change: Missense_T164I

Associated conditions / phenotypes

Beta-2-adrenoreceptor agonist, reduced response 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.