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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
SCN11A
(D1684V)
Single nucleotide variant
(missense variant)
Hereditary sensory and autonomic neuropathy type 7
+1 more
GUncertain significance
SCN11A
(I1590M)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance