RS200606811 DIAPH1
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Associated Conditions
Progressive microcephaly-seizures-cortical blindness-developmental delay syndrome
Autosomal dominant nonsyndromic hearing loss 1
Inborn genetic diseases
Progressive microcephaly-seizures-cortical blindness-developmental delay syndrome
Autosomal dominant nonsyndromic hearing loss 1
Inborn genetic diseases
Other Variants in DIAPH1