Standard

Platelet count

CAPZA2 · rs11562010

What the study found

Who was studied 166,066 European ancestry individuals.

The effect Each copy of the A allele shifted the measure 0.0264 higher (95% confidence interval 0.019-0.034); p = 9 × 10−13.

How common The A allele had a frequency of about 44% in the people studied.

Where it sits Chromosome 7, band 7q31.2 — in an intron of CAPZA2.

What each result means

A/A Two copies of the version the research linked to Platelet count. That is the strongest link of the three results. A link in a study is not a diagnosis.
A/T One copy of the version the research linked to Platelet count. That is a smaller link than two copies.
T/T No copy of the version the research linked to Platelet count. This is the starting point the study compared everyone against.
Source

Questions about rs11562010

What is rs11562010?

rs11562010 is a single position in the genome, in or near the CAPZA2 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 rs11562010 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 rs11562010 come from?

GWAS Catalog, Cell 2016, PMID:27863252. 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.

Platelet count (rs11562010). MyGeneLog™. https://www.mygenelog.com/variants/rs11562010

← See all variants