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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
MATR3
(Q209R)
Single nucleotide variant
(missense variant +1 more)
Amyotrophic lateral sclerosis
GUncertain significance
MATR3
(T436I +2 more)
Single nucleotide variant
(missense variant)
Amyotrophic lateral sclerosis
GUncertain significance