RS267607144 TRPV4

Health Risk Chr 12:109800665
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What This Variant Does
"CLNSIG=5
Associated Conditions
Neuronopathy
distal hereditary motor
autosomal dominant 8
Charcot-Marie-Tooth disease axonal type 2C
Charcot-Marie-Tooth disease
Neuromuscular disease
Inborn genetic diseases
11 conditions
TRPV4-related bone disorder
Neuronopathy
distal hereditary motor
autosomal dominant 8
Charcot-Marie-Tooth disease axonal type 2C
Charcot-Marie-Tooth disease
Neuromuscular disease
Other Variants in TRPV4
rs121912632 rs121912633 rs77975504 rs121912634 rs121912636 rs121912637 rs267607143 rs267607145 rs267607146 rs267607147
Ask Dr. Hemsworth about this variant