Standard

Shoulder impingement or rotator cuff tear

C5orf63 · rs145648292

What each result means

A/A Published research associates this genotype (two copies of the reported risk allele) with a higher likelihood of Shoulder impingement or rotator cuff tear compared to the general population. (GWAS Catalog, J Shoulder Elbow Surg 2021, PMID:33482370)
A/G Published research associates this genotype (one copy of the reported risk allele) with an intermediate association with Shoulder impingement or rotator cuff tear. (GWAS Catalog, J Shoulder Elbow Surg 2021, PMID:33482370)
G/G Published research associates this genotype with typical/baseline likelihood of Shoulder impingement or rotator cuff tear — no copies of the reported risk allele. (GWAS Catalog, J Shoulder Elbow Surg 2021, PMID:33482370)
Source

Questions about rs145648292

What is rs145648292?

rs145648292 is a single position in the genome, in or near the C5orf63 gene. Published research associates it with shoulder impingement or rotator cuff tear. A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.

Does having rs145648292 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 rs145648292 come from?

GWAS Catalog, J Shoulder Elbow Surg 2021, PMID:33482370. 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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