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Leucine-rich repeat and transmembrane domain-containing protein 2 levels

SKIC2 · rs449643

What the study found

Who was studied 10,708 European ancestry individuals.

The effect Each copy of the T allele shifted the measure 0.243 higher (95% confidence interval 0.21-0.28); p = 5 × 10−37.

How common The T allele had a frequency of about 14% in the people studied.

Where it sits Chromosome 6, band 6p21.33 — a missense change in SKIC2.

What ClinVar records

Classification Benign/Likely benign for Trichohepatoenteric syndrome 2, Malignant lymphoma, large B-cell, diffuse, Uveal melanoma; criteria provided, multiple submitters, no conflicts (2 of 4 stars, 6 submitters), last evaluated 2026-02-04. ClinVar record 356346 NM_006929.5(SKIC2):c.3212C>T (p.Ala1071Val)

What this is ClinVar's aggregate record for this position (as of its 2026-10-19 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.

What each result means

C/C No copy of the version the research linked to Leucine-rich repeat and transmembrane domain-containing protein 2 levels. This is the starting point the study compared everyone against.
C/T One copy of the version the research linked to Leucine-rich repeat and transmembrane domain-containing protein 2 levels. That is a smaller link than two copies.
T/T Two copies of the version the research linked to Leucine-rich repeat and transmembrane domain-containing protein 2 levels. That is the strongest link of the three results. A link in a study is not a diagnosis.
Source

Questions about rs449643

What is rs449643?

rs449643 is a single position in the genome, in or near the SKIC2 gene. Published research associates it with leucine-rich repeat and transmembrane domain-containing protein 2 levels. A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.

Does having rs449643 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 rs449643 come from?

GWAS Catalog, Science (New York, N.Y.) 2021, PMID:34648354. Every variant on MyGeneLog comes from public primary sources and is published with its citation and the date it was checked.

Quoting this page

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Leucine-rich repeat and transmembrane domain-containing protein 2 levels (rs449643). MyGeneLog™. https://www.mygenelog.com/variants/rs449643

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