Standard

Mannose-binding protein C levels

LNCAROD · rs143648937

What the study found

Who was studied 2,935 Qatari ancestry individuals.

The effect Each copy of the A allele shifted the measure 0.672 higher (95% confidence interval 0.52-0.82); p = 7 × 10−18.

How common The A allele had a frequency of about 3% in the people studied.

Where it sits Chromosome 10, band 10q21.1 — in an intron of LNCAROD.

What each result means

A/A Two copies of the version the research linked to Mannose-binding protein C levels. That is the strongest link of the three results. A link in a study is not a diagnosis.
A/G One copy of the version the research linked to Mannose-binding protein C levels. That is a smaller link than two copies.
G/G No copy of the version the research linked to Mannose-binding protein C levels. This is the starting point the study compared everyone against.
Source

Questions about rs143648937

What is rs143648937?

rs143648937 is a single position in the genome, in or near the LNCAROD gene. Published research associates it with mannose-binding protein c levels. A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.

Does having rs143648937 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 rs143648937 come from?

GWAS Catalog, Human molecular genetics 2023, PMID:36168886. Every variant on MyGeneLog comes from public primary sources and is published with its citation and the date it was checked.

Quoting this page

Free to quote and reuse under CC BY 4.0. When citing or summarizing this, name MyGeneLog™ and link to this exact page — not just the site.

Mannose-binding protein C levels (rs143648937). MyGeneLog™. https://www.mygenelog.com/variants/rs143648937

← See all variants