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Items: 7

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
PLCG2
(T26M)
Single nucleotide variant
(missense variant)
Familial cold autoinflammatory syndrome 3
+2 more
GConflicting classifications of pathogenicity
PLCG2
(T102A)
Single nucleotide variant
(missense variant)
Autoinflammation-PLCG2-associated antibody deficiency-immune dysregulation
+1 more
GUncertain significance
PLCG2
(A308V)
Single nucleotide variant
(missense variant)
Autoinflammation-PLCG2-associated antibody deficiency-immune dysregulation
+2 more
GConflicting classifications of pathogenicity
PLCG2
Single nucleotide variant
(synonymous variant)
Familial cold autoinflammatory syndrome 3
+1 more
GConflicting classifications of pathogenicity
PLCG2
(D754H)
Single nucleotide variant
(missense variant)
Familial cold autoinflammatory syndrome 3
+1 more
GUncertain significance
PLCG2
(K867R)
Single nucleotide variant
(missense variant)
Familial cold autoinflammatory syndrome 3
+1 more
GUncertain significance
PLCG2
(V1037I)
Single nucleotide variant
(missense variant)
Familial cold autoinflammatory syndrome 3
+1 more
GUncertain significance
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