RS202143667 CHD7
Upload your DNA to see your genotype for this variant.
Associated Conditions
Hypogonadotropic hypogonadism 5 with or without anosmia
Childhood onset hearing loss
CHARGE syndrome
Inborn genetic diseases
Hypogonadotropic hypogonadism 5 with or without anosmia
Childhood onset hearing loss
CHARGE syndrome
Inborn genetic diseases
Other Variants in CHD7