RS267607145 TRPV4

Health Risk Chr 12:109798820
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What This Variant Does
"CLNSIG=5
Associated Conditions
Charcot-Marie-Tooth disease axonal type 2C
Scapuloperoneal spinal muscular atrophy
Neuromuscular disease
Charcot-Marie-Tooth disease
Neuronopathy
distal hereditary motor
autosomal dominant
TRPV4-related disorder
Inborn genetic diseases
Charcot-Marie-Tooth disease axonal type 2C
Scapuloperoneal spinal muscular atrophy
Neuromuscular disease
Charcot-Marie-Tooth disease
Neuronopathy
distal hereditary motor
Other Variants in TRPV4
rs121912632 rs121912633 rs77975504 rs121912634 rs121912636 rs121912637 rs267607143 rs267607144 rs267607146 rs267607147
Ask Dr. Hemsworth about this variant