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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 31,434 European ancestry individuals.
The effect
Each copy of the T allele shifted the measure 0.28 lower (95% confidence interval 0.18-0.38); p = 9 × 10−9.
How common The T allele had a frequency of about 41% in the people studied.
Where it sits Chromosome 9, band 9q31.1 — in an intron of INVS.
What each result means
C/CNo copy of the version the research linked to Ganglion cell inner plexiform layer (GCIPL) thickness. This is the starting point the study compared everyone against.
C/TOne copy of the version the research linked to Ganglion cell inner plexiform layer (GCIPL) thickness. That is a smaller link than two copies.
T/TTwo copies of the version the research linked to Ganglion cell inner plexiform layer (GCIPL) thickness. That is the strongest link of the three results. A link in a study is not a diagnosis.
PLoS genetics · 2021 · PMID 33979322 · open access
Questions about rs2787394
What is rs2787394?
rs2787394 is a single position in the genome, in or near the INVS gene. Published research associates it with ganglion cell inner plexiform layer (gcipl) thickness. A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.
Does having rs2787394 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 rs2787394 come from?
GWAS Catalog, PLoS genetics 2021, PMID:33979322. 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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