RS771373457 NPR2
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What This Variant Does
"CLNSIG=4
Associated Conditions
Epilepsy
familial focal
with variable foci 2
NPR2-related disorder
Acromesomelic dysplasia 1
Maroteaux type
Tall stature-scoliosis-macrodactyly of the great toes syndrome
Epilepsy
familial focal
with variable foci 2
Acromesomelic dysplasia 1
Maroteaux type
Epilepsy
familial focal
with variable foci 2
Other Variants in NPR2