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Platelet count

MAST4 · rs61707595

What the study found

Who was studied 38,000 South Asian ancestry individuals.

The effect Each copy of the G allele shifted the measure 0.072 higher (95% confidence interval 0.052-0.092); p = 6 × 10−14.

Where it sits Chromosome 5, band 5q12.3 — in an intron of MAST4.

What each result means

A/A Published research associates this genotype with typical/baseline likelihood of Platelet count — no copies of the reported risk allele.
A/G Published research associates this genotype (one copy of the reported risk allele) with an intermediate association with Platelet count.
G/G Published research associates this genotype (two copies of the reported risk allele) with a higher likelihood of Platelet count compared to the general population.
Source

Questions about rs61707595

What is rs61707595?

rs61707595 is a single position in the genome, in or near the MAST4 gene. Published research associates it with platelet count. A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.

Does having rs61707595 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 rs61707595 come from?

GWAS Catalog, Nature communications 2024, PMID:39414775. 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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Platelet count (rs61707595). MyGeneLog™. https://www.mygenelog.com/variants/rs61707595

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