RS201384608 NLRP3
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Associated Conditions
Chronic infantile neurological
cutaneous and articular syndrome
Familial cold autoinflammatory syndrome 1
Familial amyloid nephropathy with urticaria AND deafness
Keratitis fugax hereditaria
Hearing loss
autosomal dominant 34
with or without inflammation
Cryopyrin associated periodic syndrome
Inborn genetic diseases
Chronic infantile neurological
cutaneous and articular syndrome
Familial cold autoinflammatory syndrome 1
Familial amyloid nephropathy with urticaria AND deafness
Keratitis fugax hereditaria
Other Variants in NLRP3