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Items: 4

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
KCNJ1
(D345G +2 more)
Single nucleotide variant
(missense variant)
not provided
+2 more
GUncertain significance
KCNJ1
(M338T +2 more)
Single nucleotide variant
(missense variant)
not specified
+3 more
GBenign/Likely benign
KCNJ1
(T67A +2 more)
Single nucleotide variant
(missense variant)
KCNJ1-related disorder
+2 more
GBenign/Likely benign
KCNJ1
Single nucleotide variant
(synonymous variant)
not provided
GConflicting classifications of pathogenicity
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