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Standard

Triglycerides to Total Lipids in Small VLDL percentage

RIC8B · rs10861662

Strength of the evidence

2 / 4

Its strongest genetic-study result is p = 10−31, with 4 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 C allele shifted the measure 0.02 % lower (95% confidence interval 0.02-0.02); p = 3 × 10−12.

Where it sits Chromosome 12, band 12q23.3 — in an intron of RIC8B.

How common each version is

AC
Korean KRGDB
A 65.5% · C 34.5%
Korean Korea4K
A 66.9% · C 33.1%
Korean Korea1K
A 67.3% · C 32.7%
Japanese ToMMo
A 72.0% · C 28.0%
Vietnamese
A 72.4% · C 27.6%
World gnomAD
A 82.4% · C 17.6%
World 1000 Genomes
A 81.6% · C 18.4%
World TOPMed
A 82.4% · C 17.6%

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.

What each result means

A/A No copy of the version the research linked to Triglycerides to Total Lipids in Small VLDL percentage. This is the starting point the study compared everyone against.
A/C One copy of the version the research linked to Triglycerides to Total Lipids in Small VLDL percentage. That is a smaller link than two copies.
C/C Two copies of the version the research linked to Triglycerides to Total Lipids in Small VLDL percentage. That is the strongest link of the three results. A link in a study is not a diagnosis.
Source

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Triglycerides to Total Lipids in Small VLDL percentage (rs10861662). MyGeneLog™. https://www.mygenelog.com/variants/rs10861662

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