rs1799929
NM_000015.3(NAT2):c.481C>T (p.Leu161=)
- NAT2-related disorderBenign · germline
gnomAD allele frequency 3.61e-1
rs1799929 is a genetic variant located in the NAT2 gene. dbsnp · gene
In gnomAD, rs1799929 has an overall allele frequency of 36.1%. gnomad · frequency
In ClinVar, rs1799929 is classified as Benign for NAT2-related disorder (0 review stars, germline; last evaluated 2023-12-29). clinvar · classificationclinvar · review confidenceclinvar · originclinvar · assertion date
retrieved 2026-08-03 · facts 62b3030d63ef095b · 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.