RS77975504 TRPV4
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What This Variant Does
"[OMIM:?]
Associated Conditions
Spondylometaphyseal dysplasia
Kozlowski type
Parastremmatic dwarfism
Neuromuscular disease
Skeletal dysplasia
Charcot-Marie-Tooth disease axonal type 2C
Metatropic dysplasia
Inborn genetic diseases
Neuronopathy
distal hereditary motor
autosomal dominant 8
Multiple epiphyseal dysplasia
Spondylometaphyseal dysplasia
Kozlowski type
Parastremmatic dwarfism
Other Variants in TRPV4