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Junctophilin-1 levels

F5 · rs9332635

Where this position leads

What the study found

Who was studied 10,708 European ancestry individuals.

The effect Each copy of the T allele shifted the measure 0.242 lower (95% confidence interval 0.21-0.27); p = 1 × 10⁻⁵⁷.

How common The T allele had a frequency of about 73% in the people studied.

Where it sits Chromosome 1, band 1q24.2 — in an intron of F5.

What ClinVar records

Classification Benign; criteria provided, single submitter (1 of 4 stars, 1 submitter), last evaluated 2018-11-11. ClinVar record 1240873 NM_000130.5(F5):c.5600-178A>G

What this is ClinVar's aggregate record for this position (as of its 2026-10-19 release), not a result about you. A classification describes the variant against the condition named, as laboratories submitted it. Whether a person carries this variant, and what that would mean for them, is a question for a clinical test and a genetic counsellor.

What each result means

C/C No copy of the version the research linked to Junctophilin-1 levels. This is the starting point the study compared everyone against.

C/T One copy of the version the research linked to Junctophilin-1 levels. That is a smaller link than two copies.

T/T Two copies of the version the research linked to Junctophilin-1 levels. That is the strongest link of the three results. A link in a study is not a diagnosis.

Source

Mapping the proteo-genomic convergence of human diseases

Pietzner M, Wheeler E, Carrasco-Zanini J, Cortes A, Koprulu M, Wörheide MA, Oerton E, Cook J, Stewart ID, Kerrison ND, Luan J, Raffler J

and 9 more — show all

Arnold M, Arlt W, O'Rahilly S, Kastenmüller G, Gamazon ER, Hingorani AD, Scott RA, Wareham NJ, Langenberg C

Science (New York, N.Y.) · 2021 · PMID 34648354

Questions about rs9332635

What is rs9332635?

rs9332635 is a single position in the genome, in or near the F5 gene. Published research associates it with junctophilin-1 levels. A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.

Does rs9332635 affect how medicines work?

F5 carries pharmacogenomic findings for Combined hormonal contraceptives. That is educational information, not a prescription or a dosing guide. Any decision to start, stop or change a medicine belongs with the clinician or pharmacist managing your treatment.

Does having rs9332635 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 rs9332635 come from?

GWAS Catalog, Science (New York, N.Y.) 2021, PMID:34648354. 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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Junctophilin-1 levels (rs9332635). MyGeneLog™. https://www.mygenelog.com/variants/rs9332635

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