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Color vision defects (Tritan)

WDR73 · rs145079583

What the study found

Who was studied 12 Silk Road (founder/genetic isolate) cases, 508 Silk Road (founder/genetic isolate) controls.

The effect Each copy of the G allele shifted the measure 0.344 lower (95% confidence interval 0.26-0.43); p = 9 × 10−14.

How common The G allele had a frequency of about 98% in the people studied.

Where it sits Chromosome 15, band 15q25.2 — in an intron of WDR73.

What each result means

A/A No copy of the version the research linked to Color vision defects (Tritan). This is the starting point the study compared everyone against.
A/G One copy of the version the research linked to Color vision defects (Tritan). That is a smaller link than two copies.
G/G Two copies of the version the research linked to Color vision defects (Tritan). That is the strongest link of the three results. A link in a study is not a diagnosis.
Source

Questions about rs145079583

What is rs145079583?

rs145079583 is a single position in the genome, in or near the WDR73 gene. Published research associates it with color vision defects (tritan). A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.

Does having rs145079583 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 rs145079583 come from?

GWAS Catalog, Frontiers in genetics 2023, PMID:37359372. 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.

Color vision defects (Tritan) (rs145079583). MyGeneLog™. https://www.mygenelog.com/variants/rs145079583

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