RS2548718084 TRPV4

Health Risk Chr 12:109788596
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Associated Conditions
Inborn genetic diseases
Scapuloperoneal spinal muscular atrophy
Charcot-Marie-Tooth disease axonal type 2C
Neuronopathy
distal hereditary motor
autosomal dominant 8
Inborn genetic diseases
Scapuloperoneal spinal muscular atrophy
Charcot-Marie-Tooth disease axonal type 2C
Neuronopathy
distal hereditary motor
autosomal dominant 8
Other Variants in TRPV4
rs121912632 rs121912633 rs77975504 rs121912634 rs121912636 rs121912637 rs267607143 rs267607144 rs267607145 rs267607146
Ask Dr. Hemsworth about this variant