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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
SCN11A
(L1302F)
Single nucleotide variant
(missense variant)
Hereditary sensory and autonomic neuropathy type 7
Gnot provided
SCN11A
(L811P)
Single nucleotide variant
(missense variant)
Hereditary sensory and autonomic neuropathy type 7
GPathogenic