Immune response to measles vaccine (measles-specific neutralising antibody titre)
MIR29B2CHG · rs6669384
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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.
What the study found
Who was studied 2,555 European ancestry individuals, 317 African American individuals.
The effect
The reported allele is C; the catalogue records no effect size
; p = 1 × 10−8.
How common The C allele had a frequency of about 22% in the people studied.
Where it sits Chromosome 1, band 1q32.2 — in an intron of MIR29B2CHG.
What each result means
C/CTwo copies of the version the research linked to Immune response to measles vaccine (measles-specific neutralising antibody titre). That is the strongest link of the three results. A link in a study is not a diagnosis.
C/TOne copy of the version the research linked to Immune response to measles vaccine (measles-specific neutralising antibody titre). That is a smaller link than two copies.
T/TNo copy of the version the research linked to Immune response to measles vaccine (measles-specific neutralising antibody titre). This is the starting point the study compared everyone against.
rs6669384 is a single position in the genome, in or near the MIR29B2CHG gene. Published research associates it with immune response to measles vaccine (measles-specific neutralising antibody titre). A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.
Does having rs6669384 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 rs6669384 come from?
GWAS Catalog, GWAS Catalog n.d., PMID:28289848. 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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