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Items: 4

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
KCNJ10
(R18Q)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
+6 more
GConflicting classifications of pathogenicity
PI4K2B
(W269C)
Single nucleotide variant
(missense variant +1 more)
Autism
GUncertain significance
CLTCL1
(R1165C)
Single nucleotide variant
(missense variant)
not provided
+1 more
GBenign
PLA2G6
(Y790* +4 more)
Single nucleotide variant
(nonsense)
Autism
+11 more
GConflicting classifications of pathogenicity
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