RS145303691 ACTG1
Upload your DNA to see your genotype for this variant.
Associated Conditions
Autosomal dominant nonsyndromic hearing loss 20
Baraitser-winter syndrome 2
ACTG1-related disorder
Autosomal dominant nonsyndromic hearing loss 20
Baraitser-winter syndrome 2
ACTG1-related disorder
Other Variants in ACTG1