Variant: rs2186564 

    present in Gene: AAMDC;RSF1
    present in Chromosome: 11
    Position on Chromosome: 77872220
    Alleles of this Variant: G/A

rs2186564 in AAMDC;RSF1 gene and Graves Disease 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.

rs2186564 in AAMDC;RSF1 gene and Thyrotoxic periodic paralysis PMID 31050781 2019 Two new TPP-specific susceptibility loci were identified: DCHS2 on 4q31.3 (rs1352714: odds ratio [OR], 1.58; 95% CI, 1.35-1.85; P = 1.24 × 10-8) and C11orf67 on 11q14.1 (rs2186564: OR, 1.50; 95% CI, 1.29-1.74; P = 2.80 × 10-7).