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Stands on its own.
Nothing else here links to this position yet — but the page above is the point: what the
research found, what each genotype means, and where it came from, in language you can
read. Links to conditions, drugs and the senses appear automatically if we write them.
What the study found
Who was studied 29,580 European ancestry individuals, 14,462 Asian ancestry individuals; replicated in 88,218 European ancestry individuals.
The effect
Each copy of the T allele shifted the measure 0.004 mm lower; p = 6 × 10−9.
How common The T allele had a frequency of about 77% in the people studied.
Where it sits Chromosome 15, band 15q21.1 — in an intron of FBN1.
What ClinVar records
ClassificationBenign; criteria provided, multiple submitters, no conflicts (2 of 4 stars, 2 submitters), last evaluated 2018-06-23.
ClinVar record 1291471NM_000138.5(FBN1):c.5224+111A>G
What this is ClinVar's aggregate record for this position (as of its 2026-10-12 release), not a result about you. A classification describes the variant against the condition named, as laboratories submitted it. Whether a person carries this variant, and what that would mean for them, is a question for a clinical test and a genetic counsellor.
What each result means
C/CNo copy of the version the research linked to Corneal curvature. This is the starting point the study compared everyone against.
C/TOne copy of the version the research linked to Corneal curvature. That is a smaller link than two copies.
T/TTwo copies of the version the research linked to Corneal curvature. That is the strongest link of the three results. A link in a study is not a diagnosis.
Communications biology · 2020 · PMID 32193507 · open access
Questions about rs9806595
What is rs9806595?
rs9806595 is a single position in the genome, in or near the FBN1 gene. Published research associates it with corneal curvature. A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.
Does having rs9806595 mean I will get this?
No. Common variants like this one move a probability slightly and, on their own, rarely decide anything about one person. Nothing on this page is a diagnosis, and health decisions should be made with a clinician who can see your whole picture.
Where does the information about rs9806595 come from?
GWAS Catalog, Communications biology 2020, PMID:32193507. Every variant on MyGeneLog comes from public primary sources and is published with its citation and the date it was checked.
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