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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
DST
(D4880N +6 more)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
+2 more
GUncertain significance
DST
(Q1090H +5 more)
Single nucleotide variant
(missense variant)
Hereditary sensory and autonomic neuropathy type 6
+1 more
GUncertain significance