RS370289434 TRPV4
Upload your DNA to see your genotype for this variant.
Associated Conditions
Spondylometaphyseal dysplasia
Kozlowski type
Charcot-Marie-Tooth disease axonal type 2C
Scapuloperoneal spinal muscular atrophy
Neuronopathy
distal hereditary motor
autosomal dominant 8
Metatropic dysplasia
Brachyrachia (short spine dysplasia)
Inborn genetic diseases
Spondylometaphyseal dysplasia
Kozlowski type
Charcot-Marie-Tooth disease axonal type 2C
Scapuloperoneal spinal muscular atrophy
Neuronopathy
Other Variants in TRPV4