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Items: 3

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
SLC12A2
(N690S)
Single nucleotide variant
(missense variant +1 more)
Delpire-McNeill syndrome
GUncertain significance
SLC12A2
(E1124G +1 more)
Single nucleotide variant
(missense variant +1 more)
Delpire-McNeill syndrome
GUncertain significance
SLC12A2
(V1162E +1 more)
Single nucleotide variant
(missense variant +1 more)
Delpire-McNeill syndrome
GUncertain significance
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