RS587777450 PIEZO2
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What This Variant Does
"CLNSIG=5
Associated Conditions
Gordon syndrome
Arthrogryposis- oculomotor limitation-electroretinal anomalies syndrome
Inborn genetic diseases
Fetal akinesia deformation sequence 1
Arthrogryposis multiplex congenita
Arthrogryposis
distal
with impaired proprioception and touch
Gordon syndrome
Arthrogryposis- oculomotor limitation-electroretinal anomalies syndrome
Inborn genetic diseases
Fetal akinesia deformation sequence 1
Arthrogryposis multiplex congenita
Arthrogryposis
distal
Other Variants in PIEZO2