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Items: 4

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
CLDN19
(V224E)
Single nucleotide variant
(3 prime UTR variant +1 more)
Renal hypomagnesemia 5 with ocular involvement
+1 more
GUncertain significance
CLDN19
(G101S)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
CLDN19
(W51C)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
CLDN19
(A43V)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
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