Sensitive

Restless legs syndrome

RNF8 · rs17636328

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Where this position leads

Condition: Restless Legs Syndrome

rs17636328 Condition: Restless Legs Syndrome Restless Legs Syndrome Condition rs17636328 RNF8

What each result means

A/A Published research associates this genotype (two copies of the reported risk allele) with a higher likelihood of Restless legs syndrome compared to the general population. (GWAS Catalog, Lancet Neurol 2017, PMID:29029846)
A/G Published research associates this genotype (one copy of the reported risk allele) with an intermediate association with Restless legs syndrome. (GWAS Catalog, Lancet Neurol 2017, PMID:29029846)
G/G Published research associates this genotype with typical/baseline likelihood of Restless legs syndrome — no copies of the reported risk allele. (GWAS Catalog, Lancet Neurol 2017, PMID:29029846)

Source: GWAS Catalog, Lancet Neurol 2017, PMID:29029846

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