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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 = 10−22, with 3 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 1,320,016 European ancestry individuals.
The effect
Each copy of the C allele shifted the measure 0.0162 higher (95% confidence interval 0.014-0.019); p = 4 × 10−23.
How common The C allele had a frequency of about 42% in the people studied.
Where it sits Chromosome 10, band 10q24.31 — in an intron of CWF19L1.
How common each version is
CG
KoreanKRGDB
C 5.3% · G 94.7%
KoreanKorea4K
C 5.3% · G 94.7%
KoreanKorea1K
C 5.2% · G 94.8%
Japanese ToMMo
C 4.1% · G 95.9%
Vietnamese
C 6.5% · G 93.5%
World gnomAD
C 28.8% · G 71.2%
World 1000 Genomes
C 17.2% · G 82.8%
World TOPMed
C 27.8% · G 72.2%
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.
What each result means
C/CTwo copies of the version the research linked to Total cholesterol levels. That is the strongest link of the three results. A link in a study is not a diagnosis.
C/GOne copy of the version the research linked to Total cholesterol levels. That is a smaller link than two copies.
G/GNo copy of the version the research linked to Total cholesterol levels. This is the starting point the study compared everyone against.
rs17668357 is a single position in the genome, in or near the CWF19L1 gene. Published research associates it with total cholesterol levels. A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.
Does having rs17668357 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 rs17668357 come from?
GWAS Catalog, Nature 2021, PMID:34887591. Every variant on MyGeneLog comes from public primary sources and is published with its citation and the date it was checked.
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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
Total cholesterol levels (rs17668357). MyGeneLog™. https://www.mygenelog.com/variants/rs17668357