Cysteine-rich with EGF-like domain protein 1 levels
ATP2B2 · rs4684698
0 7124Reads by AI crawlersClaude0ChatGPT0Google · Gemini0Perplexity1Meta AI0Microsoft · Copilot0Amazon2Apple0China (ByteDance, Huawei, Baidu…)0Others4Total7Counted 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 2,935 Qatari ancestry individuals.
The effect
Each copy of the G allele shifted the measure 0.202 lower (95% confidence interval 0.15-0.26); p = 7 × 10−13.
How common The G allele had a frequency of about 33% in the people studied.
Where it sits Chromosome 3, band 3p25.3 — in an intron of ATP2B2.
What each result means
C/CNo copy of the version the research linked to Cysteine-rich with EGF-like domain protein 1 levels. This is the starting point the study compared everyone against.
C/GOne copy of the version the research linked to Cysteine-rich with EGF-like domain protein 1 levels. That is a smaller link than two copies.
G/GTwo copies of the version the research linked to Cysteine-rich with EGF-like domain protein 1 levels. That is the strongest link of the three results. A link in a study is not a diagnosis.
Human molecular genetics · 2023 · PMID 36168886 · open access
Questions about rs4684698
What is rs4684698?
rs4684698 is a single position in the genome, in or near the ATP2B2 gene. Published research associates it with cysteine-rich with egf-like domain protein 1 levels. A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.
Does having rs4684698 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 rs4684698 come from?
GWAS Catalog, Human molecular genetics 2023, PMID:36168886. Every variant on MyGeneLog comes from public primary sources and is published with its citation and the date it was checked.
0 7124Reads by AI crawlersClaude0ChatGPT0Google · Gemini0Perplexity1Meta AI0Microsoft · Copilot0Amazon2Apple0China (ByteDance, Huawei, Baidu…)0Others4Total7Counted 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
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.
Cysteine-rich with EGF-like domain protein 1 levels (rs4684698). MyGeneLog™. https://www.mygenelog.com/variants/rs4684698