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Items: 4

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
C22orf31
(P97R +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
C22orf31
(K121E +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
C22orf31
(A43S +1 more)
Single nucleotide variant
(missense variant)
Intellectual disability
GUncertain significance
C22orf31
(R18Q)
Single nucleotide variant
(5 prime UTR variant +1 more)
Intellectual disability
GUncertain significance
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