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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 68,051 Icelandic ancestry cases, 68,903 Icelandic ancestry controls (includes non-array genotyped, whole-genome imputed individuals).
The effect
Each copy of the T allele carried 2.07 times the odds of Hematuria (95% confidence interval 1.60-2.67); p = 3 × 10−8.
How common The T allele had a frequency of about 0% in the people studied.
Where it sits Chromosome 2, band 2q36.2 — between genes, 17.4 kb from FAM124B.
What each result means
C/CNo copy of the version the research linked to Hematuria. This is the starting point the study compared everyone against.
C/TOne copy of the version the research linked to Hematuria. That is a smaller link than two copies.
T/TTwo copies of the version the research linked to Hematuria. That is the strongest link of the three results. A link in a study is not a diagnosis.
Human molecular genetics · 2019 · PMID 30476138 · open access
Questions about rs760545501
What is rs760545501?
rs760545501 is a single position in the genome, in or near the near FAM124B gene. Published research associates it with hematuria. A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.
Does having rs760545501 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 rs760545501 come from?
GWAS Catalog, Human molecular genetics 2019, PMID:30476138. 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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