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CD16-CD56 on Natural Killer

near NCAM1-AS2 · rs77291736

What the study found

Who was studied 3,113 Sardinian (founder/genetic isolate) ancestry individuals.

The effect Each copy of the T allele shifted the measure 1.08 lower (95% confidence interval 1-1.15); p = 7 × 10−155.

How common The T allele had a frequency of about 11% in the people studied.

Where it sits Chromosome 11, band 11q23.2 — between genes, 80.2 kb from NCAM1-AS2.

What each result means

C/C No copy of the version the research linked to CD16-CD56 on Natural Killer. This is the starting point the study compared everyone against.
C/T One copy of the version the research linked to CD16-CD56 on Natural Killer. That is a smaller link than two copies.
T/T Two copies of the version the research linked to CD16-CD56 on Natural Killer. That is the strongest link of the three results. A link in a study is not a diagnosis.
Source

Questions about rs77291736

What is rs77291736?

rs77291736 is a single position in the genome, in or near the near NCAM1-AS2 gene. Published research associates it with cd16-cd56 on natural killer. A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.

Does having rs77291736 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 rs77291736 come from?

GWAS Catalog, Nature genetics 2020, PMID:32929287. 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.

CD16-CD56 on Natural Killer (rs77291736). MyGeneLog™. https://www.mygenelog.com/variants/rs77291736

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