Variant: rs5912838 

    present in Gene: LOC107985690
    present in Chromosome: X
    Position on Chromosome: 79241621
    Alleles of this Variant: A/C

rs5912838 in LOC107985690 gene and Graves Disease PMID 23612905 2013 Robust evidence for five new Graves' disease risk loci from a staged genome-wide association analysis.

PMID 31050781 2019 Assessment of Molecular Subtypes in Thyrotoxic Periodic Paralysis and Graves Disease Among Chinese Han Adults: A Population-Based Genome-Wide Association Study.

rs5912838 in LOC107985690 gene and Thyrotoxic periodic paralysis PMID 31050781 2019 Assessment of Molecular Subtypes in Thyrotoxic Periodic Paralysis and Graves Disease Among Chinese Han Adults: A Population-Based Genome-Wide Association Study.