RS876661124 TRPV4

Health Risk Chr 12:109814507
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What This Variant Does
"CLNSIG=4
Associated Conditions
Neuronopathy
distal hereditary motor
autosomal dominant
Neuronopathy
distal hereditary motor
autosomal dominant
Other Variants in TRPV4
rs121912632 rs121912633 rs77975504 rs121912634 rs121912636 rs121912637 rs267607143 rs267607144 rs267607145 rs267607146
Ask Dr. Hemsworth about this variant