All Variants — MyGeneLog™

One specific position in the genome (an rsID), explained in plain language with what published research has found it linked to, and how strong that link actually is.

Where does new variant data come from?

The public GWAS Catalog, checked every twenty minutes, plus variants added manually after research review. Every one passes the same quality gate before publishing.

Does being listed here mean a variant causes a condition?

No. Listing reflects an association from published research, not a diagnosis or a cause. Most common variants shift probability modestly rather than determining an outcome.

Can I search this list by gene or rsID?

Yes — the search box above matches gene symbols and rsIDs as well as trait names.

Variants linked to Osteoarthritis

Body shape phenotype PC2

Body shape phenotype PC2

Trans-laminar cribrosa pressure difference

Diacylglycerol (12:0/18:0) (Model 2)

Medication use (diuretics)

Well-being spectrum (multivariate analysis)

Chronic back pain

Osteoarthritis (hip)

Medication use (agents acting on the renin-angiotensin system)

Appendicular lean mass

Medication use (anti-inflammatory and antirheumatic products, non-steroids)

Diastolic blood pressure x alcohol consumption (light vs heavy) interaction (2df test)

High density lipoprotein cholesterol levels

Total body bone mineral density

Body mass index

Hypertension

Birth weight

Height

Body mass index

Parkinson's disease

Questions about variants on this site