RS267607143 TRPV4
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What This Variant Does
"CLNSIG=5
Associated Conditions
Scapuloperoneal spinal muscular atrophy
Charcot-Marie-Tooth disease axonal type 2C
Neuronopathy
distal hereditary motor
autosomal dominant 8
Neuromuscular disease
autosomal dominant
Inborn genetic diseases
TRPV4-Associated Disorders
TRPV4-related disorder
Charcot-Marie-Tooth disease axonal type 2C
Scapuloperoneal spinal muscular atrophy
Charcot-Marie-Tooth disease axonal type 2C
Neuronopathy
distal hereditary motor
Other Variants in TRPV4