Standard
Myasthenia gravis
NR · rs3130544
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What each result means
A/A
Published research associates this genotype (two copies of the reported risk allele) with a higher likelihood of Myasthenia gravis compared to the general population. (GWAS Catalog, Ann Neurol 2012, PMID:23055271)
A/C
Published research associates this genotype (one copy of the reported risk allele) with an intermediate association with Myasthenia gravis. (GWAS Catalog, Ann Neurol 2012, PMID:23055271)
C/C
Published research associates this genotype with typical/baseline likelihood of Myasthenia gravis — no copies of the reported risk allele. (GWAS Catalog, Ann Neurol 2012, PMID:23055271)
Source: GWAS Catalog, Ann Neurol 2012, PMID:23055271
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