rs1801252
NM_000684.3(ADRB1):c.145A>G (p.Ser49Gly)
- ADRB1-related disorderBenign · germline
- Resting heart rate (RHR)association · germline
- not specifiedLikely benign · ★ · germline
- not providedLikely benign · ★ · germline
gnomAD allele frequency 1.69e-1
rs1801252 is a genetic variant located in the ADRB1 gene. dbsnp · gene
In gnomAD, rs1801252 has an overall allele frequency of 16.9%. gnomad · frequency
In ClinVar, rs1801252 is classified as Benign for ADRB1-related disorder (0 review stars, germline; last evaluated 2019-10-28). clinvar · classificationclinvar · review confidenceclinvar · originclinvar · assertion date
In ClinVar, rs1801252 is classified as association for Resting heart rate (RHR) (0 review stars, germline; last evaluated 2015-05-18). clinvar · classificationclinvar · review confidenceclinvar · originclinvar · assertion date
In ClinVar, rs1801252 is classified as Likely benign for not specified (1 review star, germline; last evaluated 2018-03-09). clinvar · classificationclinvar · review confidenceclinvar · originclinvar · assertion date
In ClinVar, rs1801252 is classified as Likely benign for not provided (1 review star, germline). clinvar · classificationclinvar · review confidenceclinvar · origin
retrieved 2026-08-03 · facts 790fe451fdc04ceb · 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.