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LRP4 · rs326214
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.
Strength of the evidence
Its strongest genetic-study result is p = 10−38, with 18 associations in the GWAS Catalog.
4: ClinVar disease-causing, reviewed by an expert panel or a guideline (3–4 stars). 3: ClinVar, several labs agreeing (2 stars), or a genetic study at p ≤ 10−50. 2: ClinVar from one lab (1 star), or p ≤ 10−20. 1: ClinVar submitted without criteria (0 stars), or genome-wide significance (p ≤ 5×10−8). The higher of the two counts. It says how solid the evidence is, not whether it matters for a particular person.
What the study found
Who was studied 34,930 East Asian ancestry individuals, 187,167 European ancestry individuals; replicated in 8,741 Chinese ancestry individuals.
The effect Each copy of the A allele shifted the measure 0.0609 lower (95% confidence interval 0.052-0.07); p = 6 × 10−39.
How common The A allele had a frequency of about 69% in the people studied.
Where it sits Chromosome 11, band 11p11.2 — a synonymous change in MADD.
What ClinVar records
Classification
Benign for Neurodevelopmental disorder with dysmorphic facies, impaired speech, and hypotonia, Deeah syndrome; criteria provided, multiple submitters, no conflicts (2 of 4 stars, 3 submitters), last evaluated 2021-09-05.
ClinVar record 1243998 NM_001376571.1(MADD):c.1041G>A (p.Glu347=)
Change history MyGeneLog™ keeps a copy of every weekly release from 2026-10-19 and compares them. This position's classification has not changed since.
What this is ClinVar's aggregate record for this position (as of its 2026-11-01 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.
How common each version is
AG
A 34.1% · G 65.9%
A 33.9% · G 66.1%
A 34.8% · G 65.2%
A 30.4% · G 69.6%
A 27.4% · G 72.6%
A 56.2% · G 43.8%
A 47.0% · G 53.0%
A 56.1% · G 43.9%
By ancestry gnomAD
A 30.7% · G 69.3%
A 68.4% · G 31.6%
A 35.7% · G 64.3%
A 53.3% · G 46.7%
A 62.4% · G 37.6%
A 70.8% · G 29.2%
A 57.0% · G 43.0%
A 75.6% · G 24.4%
The share of all copies of this position that are each version. Source: the population studies published in dbSNP (US NCBI); each row names its study. The ancestry rows are gnomAD's own groups (via Ensembl), as the survey defines them, not races.
Licensed CC BY-NC 4.0: free to read, share and adapt for non-commercial use, naming MyGeneLog™ and linking the exact page. Commercial use, including training or serving a commercial AI system, needs a licence — https://www.mygenelog.com/license
HDL cholesterol levels (rs326214). MyGeneLog™. https://www.mygenelog.com/variants/rs326214