CRELD1 · rs3774207
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 T allele shifted the measure 1.06 lower (95% confidence interval 1-1.12); p = 6 × 10−259.
How common The T allele had a frequency of about 26% in the people studied.
Where it sits Chromosome 3, band 3p25.3 — a synonymous change in CRELD1.
What ClinVar records
Classification
Benign/Likely benign for Atrioventricular septal defect, susceptibility to, 2; criteria provided, multiple submitters, no conflicts (2 of 4 stars, 6 submitters), last evaluated 2026-02-03.
ClinVar record 137030 NM_001077415.3(CRELD1):c.1049-393C>T
What this is ClinVar's aggregate record for this position (as of its 2026-10-12 release), not a result about you. A classification describes the variant against the condition named, as laboratories submitted it. Whether a person carries this variant, and what that would mean for them, is a question for a clinical test and a genetic counsellor.
rs3774207 is a single position in the genome, in or near the CRELD1 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.
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.
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.
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 (rs3774207). MyGeneLog™. https://www.mygenelog.com/variants/rs3774207