0 624Reads by AI crawlersClaude0ChatGPT0Google · Gemini0Perplexity0Meta AI0Microsoft · Copilot0Amazon2Apple0China (ByteDance, Huawei, Baidu…)0Others4Total6Counted 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.
Who was studied 3,598 Qatari ancestry cases, 2,287 Qatari ancestry controls; replicated in 4,641 Qatari ancestry cases, 3,126 Qatari ancestry controls.
The effect
The reported allele is T; the catalogue records no effect size
; p = 2 × 10−12.
How common The T allele had a frequency of about 8% in the people studied.
Where it sits Chromosome 2, band 2p24.1 — in an intron of HS1BP3.
What each result means
C/CNo copy of the version the research linked to Vitamin D deficiency. This is the starting point the study compared everyone against.
C/TOne copy of the version the research linked to Vitamin D deficiency. That is a smaller link than two copies.
T/TTwo copies of the version the research linked to Vitamin D deficiency. That is the strongest link of the three results. A link in a study is not a diagnosis.
International journal of molecular sciences · 2025 · PMID 41096749 · open access
Questions about rs62122090
What is rs62122090?
rs62122090 is a single position in the genome, in or near the HS1BP3 gene. Published research associates it with vitamin d deficiency. A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.
What conditions is rs62122090 linked to?
On MyGeneLog this position is linked to Vitamin D Deficiency and the GC Gene. The research behind each link, and its sources, are set out on that condition page.
Does having rs62122090 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 rs62122090 come from?
GWAS Catalog, International journal of molecular sciences 2025, PMID:41096749. Every variant on MyGeneLog comes from public primary sources and is published with its citation and the date it was checked.
0 624Reads by AI crawlersClaude0ChatGPT0Google · Gemini0Perplexity0Meta AI0Microsoft · Copilot0Amazon2Apple0China (ByteDance, Huawei, Baidu…)0Others4Total6Counted 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.
Vitamin D deficiency (rs62122090). MyGeneLog™. https://www.mygenelog.com/variants/rs62122090