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Cutaneous melanoma (MTAG)

AKAP12 · rs9322309

Where this position leads

Condition: Cutaneous Malignant Melanoma

rs9322309 Condition: Cutaneous Malignant Melanoma Cutaneous Malignant Melanoma Condition rs9322309 rs9322309 AKAP12

What the study found

Who was studied 380,287 European ancestry individuals; replicated in 4,089 European ancestry cases, 11,901 European ancestry controls, 44,848 cases, 1,571,864 controls.

The effect Each copy of the G allele shifted the measure 0.0492 lower (95% confidence interval 0.035-0.063); p = 3 × 10−12.

How common The G allele had a frequency of about 54% in the people studied.

Where it sits Chromosome 6, band 6q25.1 — in an intron of AKAP12.

What each result means

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

Questions about rs9322309

What is rs9322309?

rs9322309 is a single position in the genome, in or near the AKAP12 gene. Published research associates it with cutaneous melanoma (mtag). A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.

What conditions is rs9322309 linked to?

On MyGeneLog this position is linked to Cutaneous Malignant Melanoma. The research behind each link, and its sources, are set out on that condition page.

Does having rs9322309 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 rs9322309 come from?

GWAS Catalog, The Journal of investigative dermatology 2022, PMID:34813871. 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.

Cutaneous melanoma (MTAG) (rs9322309). MyGeneLog™. https://www.mygenelog.com/variants/rs9322309

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