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Items: 3

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
KCNJ11
(L262P +1 more)
Single nucleotide variant
(missense variant)
Hyperinsulinemic hypoglycemia, familial, 2
+1 more
GUncertain significance
KCNJ11
(K38E)
Single nucleotide variant
(missense variant +1 more)
Hyperinsulinemic hypoglycemia, familial, 2
GLikely pathogenic
KCNJ11
(R34H)
Single nucleotide variant
(missense variant +1 more)
Type 2 diabetes mellitus
+5 more
GPathogenic/Likely pathogenic
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