Red blood cell side fluorescence distribution width
ATAD2B · rs72796327
0 725Reads by AI crawlersClaude0ChatGPT0Google · Gemini0Perplexity0Meta AI0Microsoft · Copilot0Amazon2Apple0China (ByteDance, Huawei, Baidu…)0Others5Total7Counted by the name each crawler declares; requests found to be impersonating one are left out. Google · Gemini includes Googlebot, the search crawler whose index Google also uses for its AI features. Other search engines and bots are under Others.
Stands on its own.
Nothing else here links to this position yet — but the page above is the point: what the
research found, what each genotype means, and where it came from, in language you can
read. Links to conditions, drugs and the senses appear automatically if we write them.
What the study found
Who was studied 30,565 European ancestry individuals.
The effect
Each copy of the C allele shifted the measure 0.146 SD units lower (95% confidence interval 0.12-0.17); p = 5 × 10−36.
How common The C allele had a frequency of about 13% in the people studied.
Where it sits Chromosome 2, band 2p23.3 — in an intron of ATAD2B.
What each result means
C/CTwo copies of the version the research linked to Red blood cell side fluorescence distribution width. That is the strongest link of the three results. A link in a study is not a diagnosis.
C/TOne copy of the version the research linked to Red blood cell side fluorescence distribution width. That is a smaller link than two copies.
T/TNo copy of the version the research linked to Red blood cell side fluorescence distribution width. This is the starting point the study compared everyone against.
Nature communications · 2023 · PMID 37596262 · open access
Questions about rs72796327
What is rs72796327?
rs72796327 is a single position in the genome, in or near the ATAD2B gene. Published research associates it with red blood cell side fluorescence distribution width. A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.
Does having rs72796327 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 rs72796327 come from?
GWAS Catalog, Nature communications 2023, PMID:37596262. Every variant on MyGeneLog comes from public primary sources and is published with its citation and the date it was checked.
0 725Reads by AI crawlersClaude0ChatGPT0Google · Gemini0Perplexity0Meta AI0Microsoft · Copilot0Amazon2Apple0China (ByteDance, Huawei, Baidu…)0Others5Total7Counted by the name each crawler declares; requests found to be impersonating one are left out. Google · Gemini includes Googlebot, the search crawler whose index Google also uses for its AI features. Other search engines and bots are under Others.
Quoting this page
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Red blood cell side fluorescence distribution width (rs72796327). MyGeneLog™. https://www.mygenelog.com/variants/rs72796327