rs1056836
NM_000104.4(CYP1B1):c.1294= (p.Leu432=)
- Congenital glaucomaBenign · ★ · germline
- Anterior segment dysgenesis 6 (ASGD6)Benign · ★ · germline
- Glaucoma 3ABenign · ★ · germline
- not providedLikely benign · ★★ · germline
- not specifiedBenign · ★★ · germline
rs1056836 is a genetic variant located in the CYP1B1 gene. dbsnp · gene
In ClinVar, rs1056836 is classified as Benign for Congenital glaucoma (1 review star, germline; last evaluated 2025-02-03). clinvar · classificationclinvar · review confidenceclinvar · originclinvar · assertion date
In ClinVar, rs1056836 is classified as Benign for Anterior segment dysgenesis 6 (ASGD6) (1 review star, germline; last evaluated 2021-07-30). clinvar · classificationclinvar · review confidenceclinvar · originclinvar · assertion date
In ClinVar, rs1056836 is classified as Benign for Glaucoma 3A (1 review star, germline; last evaluated 2021-07-30). clinvar · classificationclinvar · review confidenceclinvar · originclinvar · assertion date
In ClinVar, rs1056836 is classified as Likely benign for not provided (2 review stars, germline; last evaluated 2016-10-01). clinvar · classificationclinvar · review confidenceclinvar · originclinvar · assertion date
In ClinVar, rs1056836 is classified as Benign for not specified (2 review stars, germline; last evaluated 2021-12-03). clinvar · classificationclinvar · review confidenceclinvar · originclinvar · assertion date
retrieved 2026-08-03 · facts fdb1f7e5681a3fd0 · 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.