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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
BCAP31
(V237L +1 more)
Single nucleotide variant
(missense variant)
Severe motor and intellectual disabilities-sensorineural deafness-dystonia syndrome
GUncertain significance
BCAP31
Deletion
(intron variant)
Severe motor and intellectual disabilities-sensorineural deafness-dystonia syndrome
GUncertain significance