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Items: 10

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
ABCC8
(S1386F +3 more)
Single nucleotide variant
(missense variant +1 more)
not provided
+1 more
GPathogenic
ABCC8
Single nucleotide variant
(non-coding transcript variant +1 more)
Hyperinsulinemic hypoglycemia, familial, 1
+5 more
GPathogenic
ABCC8
Single nucleotide variant
(splice donor variant)
Hyperinsulinemic hypoglycemia, familial, 1
GLikely pathogenic
ABCC8
(D1191fs +3 more)
Duplication
(frameshift variant +1 more)
Hyperinsulinemic hypoglycemia, familial, 1
GPathogenic
ABCC8
(Q933* +3 more)
Single nucleotide variant
(nonsense +1 more)
not provided
+2 more
GPathogenic
ABCC8
(L723del +2 more)
Deletion
(inframe_deletion +1 more)
Hyperinsulinemic hypoglycemia, familial, 1
+2 more
GConflicting classifications of pathogenicity
ABCC8
Deletion
(inframe_deletion +1 more)
Hyperinsulinemic hypoglycemia, familial, 1
GUncertain significance
ABCC8
(E501K +1 more)
Single nucleotide variant
(missense variant +1 more)
Hyperinsulinemic hypoglycemia, familial, 1
+3 more
GPathogenic/Likely pathogenic
ABCC8
(G315R +1 more)
Single nucleotide variant
(missense variant +1 more)
Hyperinsulinemic hypoglycemia, familial, 1
+5 more
GConflicting classifications of pathogenicity
ABCC8
(W231*)
Single nucleotide variant
(nonsense +1 more)
Hyperinsulinemic hypoglycemia, familial, 1
+1 more
GPathogenic/Likely pathogenic
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