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Items: 4

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
MAP1B
(M127I +1 more)
Single nucleotide variant
(missense variant +1 more)
not provided
GUncertain significance
LOC129994023, MAP1B
(K405E +1 more)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
MAP1B
(V1195E +1 more)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
MAP1B
(Y1704C +1 more)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
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