Standard

Triglycerides to Total Lipids in Very Large HDL percentage

SERPINA1 · rs709932

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

2 / 4

Its strongest genetic-study result is p = 10⁻³⁶, with 16 associations in the GWAS Catalog.

How this is scored

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 434,646 British ancestry individuals, 8,796 British Central/South Asian individuals, 6,573 British African individuals.

The effect Each copy of the T allele shifted the measure 0.02 % lower (95% confidence interval 0.02-0.02); p = 2 × 10⁻¹¹.

Where it sits Chromosome 14, band 14q32.13 — a missense change in SERPINA1.

What ClinVar records

Classification Benign/Likely benign for PI M4, PI M2, Alpha-1-antitrypsin deficiency, Inborn genetic diseases; criteria provided, multiple submitters, no conflicts (2 of 4 stars, 16 submitters), last evaluated 2026-02-04. ClinVar record 17957 NM_001127701.1(SERPINA1):c.374G>A (p.Arg125His)

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

CT

Korean KRGDB

C 81.5% · T 18.6%

Korean Korea4K

C 81.8% · T 18.2%

Japanese ToMMo

C 75.8% · T 24.2%

Vietnamese

C 72.3% · T 27.7%

World gnomAD

C 87.4% · T 12.6%

World 1000 Genomes

C 84.0% · T 16.1%

World TOPMed

C 88.3% · T 11.7%

By ancestry gnomAD

East Asian

C 78.0% · T 22.1%

European (non-Finnish)

C 83.9% · T 16.1%

African / African American

C 96.1% · T 3.9%

South Asian

C 72.0% · T 28.0%

Admixed American (Latino)

C 87.9% · T 12.1%

Middle Eastern

C 77.2% · T 22.8%

Finnish

C 87.9% · T 12.1%

Ashkenazi Jewish

C 83.8% · T 16.2%

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.

What each result means

C/C No copy of the version the research linked to Triglycerides to Total Lipids in Very Large HDL percentage. This is the starting point the study compared everyone against.

C/T One copy of the version the research linked to Triglycerides to Total Lipids in Very Large HDL percentage. That is a smaller link than two copies.

T/T Two copies of the version the research linked to Triglycerides to Total Lipids in Very Large HDL percentage. That is the strongest link of the three results. A link in a study is not a diagnosis.

Source

A genetic map of human metabolism across the allele frequency spectrum

Zoodsma M, Beuchel C, Yasmeen S, Kohleick L, Nepal A, Koprulu M, Kronenberg F, Mayr M, Williamson A, Pietzner M, Langenberg C

Nature genetics · 2025 · PMID 41044249 · open access

Quoting this page

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

Triglycerides to Total Lipids in Very Large HDL percentage (rs709932). MyGeneLog™. https://www.mygenelog.com/variants/rs709932

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