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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
WNK1
(P2127fs +3 more)
Deletion
(frameshift variant)
Hereditary motor and sensory neuropathy
GUncertain significance
DRP2
Single nucleotide variant
(intron variant)
Hereditary motor and sensory neuropathy
GUncertain significance