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rs1042713

NM_000024.6(ADRB2):c.46G>A (p.Gly16Arg)

ADRB2missense variantp.Gly16Argsingle nucleotide variant
ClinVar by condition
  • salmeterol response - EfficacyDrug response · ★★★ · germline

gnomAD allele frequency 4.27e-1

rs1042713 is a genetic variant located in the ADRB2 gene. dbsnp · gene

In gnomAD, rs1042713 has an overall allele frequency of 42.7%. gnomad · frequency

In ClinVar, rs1042713 is classified as Drug response (efficacy) for salmeterol response (3 review stars, germline; last evaluated 2021-03-24). clinvar · classificationclinvar · review confidenceclinvar · originclinvar · assertion date

Sources

retrieved 2026-08-03 · facts d51f07c090496786 · meta/llama-3.1-8b-instruct · prompt 4.0.1 · schema 3.0.0

Educational information only — not medical advice, a diagnosis, or a clinical interpretation. A variant's significance can be uncertain, conflicting, or dependent on your full clinical and family context. Consult a qualified genetics professional or genetic counselor before drawing any conclusion.