Variant: rs1443438 

    present in Gene: PTCSC2
    present in Chromosome: 9
    Position on Chromosome: 97787746
    Alleles of this Variant: T/A;C

rs1443438 in PTCSC2 gene and AUTOIMMUNE DISEASE, MULTISYSTEM, INFANTILE-ONSET, 1 PMID 30595370 2019 Leveraging Polygenic Functional Enrichment to Improve GWAS Power.

rs1443438 in PTCSC2 gene and AUTOIMMUNE DISEASE, MULTISYSTEM, INFANTILE-ONSET, 2 PMID 30595370 2019 Leveraging Polygenic Functional Enrichment to Improve GWAS Power.

rs1443438 in PTCSC2 gene and AUTOIMMUNE DISEASE, SUSCEPTIBILITY TO, 6 PMID 30595370 2019 Leveraging Polygenic Functional Enrichment to Improve GWAS Power.

rs1443438 in PTCSC2 gene and Autoimmune Diseases PMID 30595370 2019 Leveraging Polygenic Functional Enrichment to Improve GWAS Power.

rs1443438 in PTCSC2 gene and Hypothyroidism PMID 22493691 2012 Novel associations for hypothyroidism include known autoimmune risk loci.

rs1443438 in PTCSC2 gene and Polysomnography PMID 23251661 2012 Novel genetic loci identified for the pathophysiology of childhood obesity in the Hispanic population.

rs1443438 in PTCSC2 gene and Thyroid carcinoma PMID 23894154 2013 Genome-wide association study on differentiated thyroid cancer.

rs1443438 in PTCSC2 gene and Thyroid stimulating hormone measurement PMID 23251661 2012 Novel genetic loci identified for the pathophysiology of childhood obesity in the Hispanic population.