KRT18P13

Genes:

• C9orf156
• FOXE1
• KRT18P13
• XPA

GWAS Disease/Phenotype:

• Hypothyroidism
• Serum thyroid-stimulating hormone levels

Genes:

• C9orf156
• C9orf97
• FOXE1
• HEMGN
• KRT18P13
• NCBP1
• TMOD1
• XPA

GWAS Disease/Phenotype:

• Thyroid cancer
• Thyroid cancer (Papillary, radiation-related)