RS794729667 ATP6V1B2
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What This Variant Does
"CLNSIG=5
Associated Conditions
Autosomal dominant deafness - onychodystrophy syndrome
Neurodevelopmental delay
Zimmermann-Laband syndrome 2
Autosomal dominant deafness - onychodystrophy syndrome
Autosomal dominant deafness - onychodystrophy syndrome
Neurodevelopmental delay
Zimmermann-Laband syndrome 2
Autosomal dominant deafness - onychodystrophy syndrome
Other Variants in ATP6V1B2