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Links from Gene

Items: 4

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
CLDN19
(G17fs)
Duplication
(frameshift variant +1 more)
Renal hypomagnesemia 5 with ocular involvement
GUncertain significance
CLDN19
(R186C)
Indel
(3 prime UTR variant +2 more)
not provided
GUncertain significance
CLDN19
(G101S)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
CLDN19
(A43V)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
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