rs1801253
NM_000684.3(ADRB1):c.1165G>C (p.Gly389Arg)
- ADRB1-related disorderBenign · germline
- Pulmonary disease, chronic obstructive, susceptibility toassociation · germline
- not providedBenign · germline
gnomAD allele frequency 6.98e-1
rs1801253 is a genetic variant located in the ADRB1 gene. dbsnp · gene
In gnomAD, rs1801253 has an overall allele frequency of 69.8%. gnomad · frequency
In ClinVar, rs1801253 is classified as Benign for ADRB1-related disorder (0 review stars, germline; last evaluated 2019-10-17). clinvar · classificationclinvar · review confidenceclinvar · originclinvar · assertion date
In ClinVar, rs1801253 is classified as association for Pulmonary disease, chronic obstructive, susceptibility to (0 review stars, germline; last evaluated 2022-07-05). clinvar · classificationclinvar · review confidenceclinvar · originclinvar · assertion date
In ClinVar, rs1801253 is classified as Benign for not provided (0 review stars, germline; last evaluated 2007-04-01). clinvar · classificationclinvar · review confidenceclinvar · originclinvar · assertion date
retrieved 2026-08-03 · facts 9b7f50479ae0d1be · 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.