RS769317780 TRNT1
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Associated Conditions
Congenital sideroblastic anemia-B-cell immunodeficiency-periodic fever-developmental delay syndrome
Retinal dystrophy
TRNT1-related disorder
Inborn genetic diseases
Congenital sideroblastic anemia-B-cell immunodeficiency-periodic fever-developmental delay syndrome
Retinal dystrophy
TRNT1-related disorder
Inborn genetic diseases
Other Variants in TRNT1