rs1051730
NM_000743.5(CHRNA3):c.645C>T (p.Tyr215=)
- Lung cancer susceptibility 2 (LNCR2)Risk factor · germline
- SMOKING AS A QUANTITATIVE TRAIT LOCUS 3 (SQTL3)Risk factor · germline
- not providedBenign · ★ · germline
gnomAD allele frequency 2.58e-1
rs1051730 is a genetic variant located in the CHRNA3 gene. dbsnp · gene
In gnomAD, rs1051730 has an overall allele frequency of 25.8%. gnomad · frequency
In ClinVar, rs1051730 is classified as Risk factor for Lung cancer susceptibility 2 (LNCR2) (0 review stars, germline; last evaluated 2008-05-01). clinvar · classificationclinvar · review confidenceclinvar · originclinvar · assertion date
In ClinVar, rs1051730 is classified as Risk factor for SMOKING AS A QUANTITATIVE TRAIT LOCUS 3 (SQTL3) (0 review stars, germline; last evaluated 2008-05-01). clinvar · classificationclinvar · review confidenceclinvar · originclinvar · assertion date
In ClinVar, rs1051730 is classified as Benign for not provided (1 review star, germline; last evaluated 2025-02-03). clinvar · classificationclinvar · review confidenceclinvar · originclinvar · assertion date
retrieved 2026-08-03 · facts 9c393106217ffa78 · 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.