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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
TENM4
(L2223P)
Single nucleotide variant
(missense variant)
Tremor, hereditary essential, 5
GUncertain significance
TENM4
(R1561W)
Single nucleotide variant
(missense variant)
Tremor, hereditary essential, 5
GUncertain significance