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Transmembrane glycoprotein NMB levels

KLHL7 · rs858267

What the study found

Who was studied 997 European ancestry individuals; replicated in 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals.

The effect Each copy of the T allele shifted the measure 1.03 higher (95% confidence interval 0.75-1.31); p = 8 × 10−13.

Where it sits Chromosome 7, band 7p15.3 — in an intron of KLHL7.

What each result means

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

Questions about rs858267

What is rs858267?

rs858267 is a single position in the genome, in or near the KLHL7 gene. Published research associates it with transmembrane glycoprotein nmb levels. A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.

Does having rs858267 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 rs858267 come from?

GWAS Catalog, Nature communications 2017, PMID:28240269. 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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Transmembrane glycoprotein NMB levels (rs858267). MyGeneLog™. https://www.mygenelog.com/variants/rs858267

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