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Items: 3

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
ARHGAP31
(H48Y)
Single nucleotide variant
(missense variant)
Adams-Oliver syndrome 1
+1 more
GUncertain significance
ARHGAP31
(S249G)
Single nucleotide variant
(missense variant)
Adams-Oliver syndrome 1
GUncertain significance
ARHGAP31
(A1003T)
Single nucleotide variant
(missense variant)
Adams-Oliver syndrome 1
GUncertain significance
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