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Items: 12

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
GCK
(R392C +5 more)
Single nucleotide variant
(missense variant)
Monogenic diabetes
GPathogenic
GCK
(S383L +5 more)
Single nucleotide variant
(missense variant)
Monogenic diabetes
GPathogenic
GCK
(G318R +2 more)
Single nucleotide variant
(missense variant +1 more)
Monogenic diabetes
+1 more
GPathogenic/Likely pathogenic
GCK
(L313fs +2 more)
Deletion
(frameshift variant +1 more)
Maturity-onset diabetes of the young type 2
GPathogenic
GCK
(I292T +2 more)
Single nucleotide variant
(missense variant +1 more)
not provided
+1 more
GConflicting classifications of pathogenicity
GCK
(G261R +2 more)
Single nucleotide variant
(missense variant)
Monogenic diabetes
GPathogenic
GCK
(Y213* +2 more)
Duplication
(nonsense)
Maturity-onset diabetes of the young type 2
+1 more
GPathogenic/Likely pathogenic
GCK
(A201S +2 more)
Single nucleotide variant
(missense variant)
Monogenic diabetes
GPathogenic
GCK
Single nucleotide variant
(intron variant)
Maturity-onset diabetes of the young type 2
+1 more
GUncertain significance
GCK
(L184P +2 more)
Single nucleotide variant
(missense variant)
Maturity-onset diabetes of the young type 2
GLikely pathogenic
GCK
(F150S +2 more)
Single nucleotide variant
(missense variant)
Monogenic diabetes
GPathogenic
GCK
(F132V +2 more)
Single nucleotide variant
(missense variant)
Maturity-onset diabetes of the young type 2
GUncertain significance
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