Sensitive

Branchiootorenal syndrome 1

EYA1 · rs529483320

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.

Strength of the evidence

There is no record yet to score this position by (a ClinVar disease classification or a genome-wide significant study). That is not the same as weak evidence.

How this is scored

4: ClinVar disease-causing, reviewed by an expert panel or a guideline (3–4 stars). 3: ClinVar, several labs agreeing (2 stars), or a genetic study at p ≤ 10⁻⁵⁰. 2: ClinVar from one lab (1 star), or p ≤ 10⁻²⁰. 1: ClinVar submitted without criteria (0 stars), or genome-wide significance (p ≤ 5×10⁻⁸). The higher of the two counts. It says how solid the evidence is, not whether it matters for a particular person.

What ClinVar records

Classification Likely benign for EYA1-related disorder, Melnick-Fraser syndrome; criteria provided, multiple submitters, no conflicts (2 of 4 stars, 3 submitters), last evaluated 2024-09-17. ClinVar record 1200303 NM_000503.6(EYA1):c.678C>T (p.Tyr226=)

Classification Pathogenic for Branchiootorenal syndrome 1, EYA1-related disorders; criteria provided, multiple submitters, no conflicts (2 of 4 stars, 2 submitters), last evaluated 2020-02-18. ClinVar record 807414 NM_000503.6(EYA1):c.678C>A (p.Tyr226Ter)

Classification Pathogenic for Melnick-Fraser syndrome; criteria provided, single submitter (1 of 4 stars, 1 submitter), last evaluated 2024-06-03. ClinVar record 2136681 NM_000503.6(EYA1):c.678C>G (p.Tyr226Ter)

Change history MyGeneLog™ keeps a copy of every weekly release from 2026-10-19 and compares them. This position's classification has not changed since.

What this is ClinVar's aggregate record for this position (as of its 2026-10-19 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

G/G No copy of the version ClinVar lists as disease-causing for Branchiootorenal syndrome 1. This is the usual result. (ClinVar VCV000807414, criteria provided, multiple submitters, no conflicts)

G/T One copy of the version ClinVar lists as disease-causing for Branchiootorenal syndrome 1. Some conditions need only one copy; for others, one copy makes a person a carrier who is usually healthy but can pass it on. A genetic counsellor can say which applies. (ClinVar VCV000807414, criteria provided, multiple submitters, no conflicts)

T/T Two copies of the version ClinVar lists as disease-causing for Branchiootorenal syndrome 1. A result like this should be confirmed by a medical genetic test and talked through with a doctor; consumer DNA files can misread rare variants. (ClinVar VCV000807414, criteria provided, multiple submitters, no conflicts)

Source: ClinVar VCV000807414, criteria provided, multiple submitters, no conflicts

Questions about rs529483320

What is rs529483320?

rs529483320 is a single position in the genome, in or near the EYA1 gene. Published research associates it with branchiootorenal syndrome 1. A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.

Does having rs529483320 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 rs529483320 come from?

ClinVar VCV000807414, criteria provided, multiple submitters, no conflicts. Every variant on MyGeneLog comes from public primary sources and is published with its citation and the date it was checked.

Quoting this page

Free to quote and reuse under CC BY 4.0. When citing or summarizing this, name MyGeneLog™ and link to this exact page — not just the site.

Branchiootorenal syndrome 1 (rs529483320). MyGeneLog™. https://www.mygenelog.com/variants/rs529483320

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