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Items: 3

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
SLC12A2
(A159V)
Single nucleotide variant
(missense variant +1 more)
Kilquist syndrome
+1 more
GConflicting classifications of pathogenicity
SLC12A2
(S965Y)
Single nucleotide variant
(missense variant +1 more)
Kilquist syndrome
+2 more
GConflicting classifications of pathogenicity
SLC12A2
(T1045I +1 more)
Single nucleotide variant
(missense variant +1 more)
Inborn genetic diseases
+1 more
GConflicting classifications of pathogenicity
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