RS200556378 ATR
Upload your DNA to see your genotype for this variant.
Associated Conditions
Seckel syndrome 1
Familial cutaneous telangiectasia and oropharyngeal predisposition cancer syndrome
Inborn genetic diseases
Seckel syndrome 1
Familial cutaneous telangiectasia and oropharyngeal predisposition cancer syndrome
Inborn genetic diseases
Other Variants in ATR