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Items: 4

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
TENM4
(I2519M)
Single nucleotide variant
(missense variant)
Tremor, hereditary essential, 5
GUncertain significance
TENM4
(R1632H)
Single nucleotide variant
(missense variant)
not provided
+1 more
GConflicting classifications of pathogenicity
TENM4
(E376K)
Single nucleotide variant
(missense variant)
Tremor, hereditary essential, 5
GUncertain significance
TENM4
(D116N)
Single nucleotide variant
(missense variant)
Tremor, hereditary essential, 5
GUncertain significance
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