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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
ARHGAP5
(L37V)
Single nucleotide variant
(missense variant)
ARHGAP5-related disorder
GUncertain significance
ARHGAP5
(A229fs)
Deletion
(frameshift variant)
ARHGAP5-related disorder
GUncertain significance