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Items: 4

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
GRM1
(R358K)
Single nucleotide variant
(missense variant)
not provided
+1 more
GUncertain significance
GRM1
(N389H)
Single nucleotide variant
(missense variant)
Spinocerebellar ataxia 44
GUncertain significance
GRM1
(N956I)
Single nucleotide variant
(missense variant +1 more)
Spinocerebellar ataxia 44
GUncertain significance
ABRACL, ADAT2
+49 more
Copy number loss
not provided
GPathogenic
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