RS139833874 NLRP3
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Associated Conditions
Familial amyloid nephropathy with urticaria AND deafness
Chronic infantile neurological
cutaneous and articular syndrome
Familial cold autoinflammatory syndrome 1
Cryopyrin associated periodic syndrome
Hearing loss
autosomal dominant 34
with or without inflammation
Keratitis fugax hereditaria
NLRP3-related disorder
Familial amyloid nephropathy with urticaria AND deafness
Chronic infantile neurological
cutaneous and articular syndrome
Familial cold autoinflammatory syndrome 1
Cryopyrin associated periodic syndrome
Other Variants in NLRP3