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IDP dMRI TBSS MO Pontine crossing tract

ROBO3 · rs4935898

What the study found

Who was studied 20,860 British ancestry individuals; replicated in 10,496 British ancestry individuals.

The effect Each copy of the A allele shifted the measure 0.293 lower (95% confidence interval 0.25-0.34); p = 5 × 10−37.

How common The A allele had a frequency of about 5% in the people studied.

Where it sits Chromosome 11, band 11q24.2 — a missense change in ROBO3.

What ClinVar records

Classification Benign for Gaze palsy, familial horizontal, with progressive scoliosis 1; criteria provided, multiple submitters, no conflicts (2 of 4 stars, 2 submitters), last evaluated 2018-01-13. ClinVar record 303236 NM_022370.4(ROBO3):c.1267G>A (p.Val423Met)

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

A/A Two copies of the version the research linked to IDP dMRI TBSS MO Pontine crossing tract. That is the strongest link of the three results. A link in a study is not a diagnosis.
A/G One copy of the version the research linked to IDP dMRI TBSS MO Pontine crossing tract. That is a smaller link than two copies.
G/G No copy of the version the research linked to IDP dMRI TBSS MO Pontine crossing tract. This is the starting point the study compared everyone against.
Source

Questions about rs4935898

What is rs4935898?

rs4935898 is a single position in the genome, in or near the ROBO3 gene. Published research associates it with idp dmri tbss mo pontine crossing tract. A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.

Does having rs4935898 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 rs4935898 come from?

GWAS Catalog, Nature neuroscience 2021, PMID:33875891. Every variant on MyGeneLog comes from public primary sources and is published with its citation and the date it was checked.

Quoting this page

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IDP dMRI TBSS MO Pontine crossing tract (rs4935898). MyGeneLog™. https://www.mygenelog.com/variants/rs4935898

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