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Items: 3

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
NLRP3
(V198M +1 more)
Single nucleotide variant
(missense variant)
Familial cold autoinflammatory syndrome
+11 more
GConflicting classifications of pathogenicity
NLRP3
Single nucleotide variant
(synonymous variant)
Chronic infantile neurological, cutaneous and articular syndrome
+6 more
GBenign
NLRP3
Single nucleotide variant
(synonymous variant)
not specified
+6 more
GBenign
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