rs6265
NM_001709.5(BDNF):c.196G>A (p.Val66Met)
- Memory impairment, susceptibility tonot provided · germline
- Post-traumatic stress disorder (PTSD)Likely risk allele · inherited
- not providedBenign · ★★ · germline
- not specifiedBenign · ★★ · germline
gnomAD allele frequency 1.52e-1
In gnomAD, rs6265 has an overall allele frequency of 15.2%. gnomad · frequency
In ClinVar, rs6265 is classified as not provided for Memory impairment, susceptibility to (0 review stars, germline; last evaluated 2025-04-03). clinvar · classificationclinvar · review confidenceclinvar · originclinvar · assertion date
In ClinVar, rs6265 is classified as Likely risk allele (risk factor) for Post-traumatic stress disorder (PTSD) (0 review stars, inherited; last evaluated 2023-12-11). clinvar · classificationclinvar · review confidenceclinvar · originclinvar · assertion date
In ClinVar, rs6265 is classified as Benign for not provided (2 review stars, germline; last evaluated 2025-02-03). clinvar · classificationclinvar · review confidenceclinvar · originclinvar · assertion date
In ClinVar, rs6265 is classified as Benign for not specified (2 review stars, germline; last evaluated 2013-06-18). clinvar · classificationclinvar · review confidenceclinvar · originclinvar · assertion date
retrieved 2026-08-03 · facts cd56825d520771b4 · 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.