Fetal hemoglobin in Sickle cell disease (HbSS or HbSB0) (conditional analysis)
near OR52J3 · rs72873904
0 22Reads by AI crawlersClaude0ChatGPT0Google · Gemini0Perplexity0Meta AI0Microsoft · Copilot0Amazon0Apple0China (ByteDance, Huawei, Baidu…)0Others2Total2Counted 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 584 African American individuals.
The effect
Each copy of the T allele shifted the measure 0.467 higher (95% confidence interval 0.3-0.63); p = 4 × 10−8.
What each result means
C/CNo copy of the version the research linked to Fetal hemoglobin in Sickle cell disease (HbSS or HbSB0) (conditional analysis). This is the starting point the study compared everyone against.
C/TOne copy of the version the research linked to Fetal hemoglobin in Sickle cell disease (HbSS or HbSB0) (conditional analysis). That is a smaller link than two copies.
T/TTwo copies of the version the research linked to Fetal hemoglobin in Sickle cell disease (HbSS or HbSB0) (conditional analysis). That is the strongest link of the three results. A link in a study is not a diagnosis.
rs72873904 is a single position in the genome, in or near the near OR52J3 gene. Published research associates it with fetal hemoglobin in sickle cell disease (hbss or hbsb0) (conditional analysis). A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.
Does having rs72873904 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 rs72873904 come from?
GWAS Catalog, Blood advances 2021, PMID:34283174. Every variant on MyGeneLog comes from public primary sources and is published with its citation and the date it was checked.
0 22Reads by AI crawlersClaude0ChatGPT0Google · Gemini0Perplexity0Meta AI0Microsoft · Copilot0Amazon0Apple0China (ByteDance, Huawei, Baidu…)0Others2Total2Counted 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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Fetal hemoglobin in Sickle cell disease (HbSS or HbSB0) (conditional analysis) (rs72873904). MyGeneLog™. https://www.mygenelog.com/variants/rs72873904